Abstract: A pneumatic excavator is configured to be pneumatically actuated using a safety mechanism, and includes a primary actuator; a secondary actuator fluidly coupled to the primary actuator; a flow valve fluidly coupled to the primary actuator; a shuttle valve fluidly coupled to the primary actuator, the secondary actuator and the flow valve; and a barrel coupled to an egress of the flow valve, the barrel defining an outlet of the pneumatic excavator. Actuating the primary and secondary actuators causes compressed air to be transmitted from the secondary actuator to the primary actuator and then to the flow valve to open the flow valve such that the compressed air exits through the outlet. Actuating one actuator and not the other causes the compressed air to be transmitted to the exit port of the shuttle valve and then to the flow valve to close the flow valve and prevent air flow therethrough.

Abstract: A pneumatic excavator includes: a barrel with an ingress configured to be fluidly connected to a supply of compressed air and an egress; an actuator; a releasable coupling to lock the actuator to the barrel in a plurality positions; and a flow valve fixedly arranged to the barrel, the flow valve in a communicative coupling with the actuator by an actuation conduit. The actuation conduit is flexible and slaved by an adjustment movement of the releasable coupling and actuator along the barrel to thereby maintain the communicative coupling therebetween. When the actuator is actuated, the actuation conduit sends causes the flow valve to open and the compressed air passes through the flow valve and exits the pneumatic excavator, and when the actuator is released, the actuation conduit sends a signal to the flow valve to close to prevent the compressed air from passing through the flow valve.

Abstract: A pneumatic excavator for delivering pulsed compressed air includes an actuator; a controller valve; a flow valve; a barrel defining an outlet of the excavator; and a pulse control line extending between the controller valve and a port downstream from an egress of the flow valve. As compressed air flows through the egress of the flow valve, the pulse control line is pressurized and shifts the controller valve to an actuated position, causing the compressed air from the actuator to close the flow valve, thus preventing the air flow from passing through a primary flow passage and through the outlet. The pulse control line being no longer pressurized by the air flow, then causes the controller valve to move to an unactuated position to cause compressed air from the actuator open the flow valve and permit the air flow through the outlet and again pressurize the pulse control line.

Abstract: A chemical delivery system with dilution control includes a chemical delivery manifold with eductors each fluidly coupled to a valve configured to operate independently to selectively control flow of a motive fluid through a respective eductor. Metering devices are coupled to concentrated chemical lines and configured to control a rate of dispensing of the concentrated chemical passing therethrough to each of the eductors. Concentrated chemical flow rate sensors are coupled to each of these individual concentrated chemical lines and configured to measure a flow rate of the concentrated chemicals therethrough. A control unit receives a measured flow rate from each flow rate sensor and causes a respective metering device to adjust the rate of dispensing for one or more concentrated chemicals to control the flow rates of the concentrated chemicals and thereby individually control a dilution of each concentrated chemical in the motive fluid.

Abstract: A pneumatic excavator is configured to be pneumatically actuated using a safety mechanism, and includes a primary actuator; a secondary actuator fluidly coupled to the primary actuator; a flow valve fluidly coupled to the primary actuator; a shuttle valve fluidly coupled to the primary actuator, the secondary actuator and the flow valve; and a barrel coupled to an egress of the flow valve, the barrel defining an outlet of the pneumatic excavator. Actuating the primary and secondary actuators causes compressed air to be transmitted from the secondary actuator to the primary actuator and then to the flow valve to open the flow valve such that the compressed air exits through the outlet. Actuating one actuator and not the other causes the compressed air to be transmitted to the exit port of the shuttle valve and then to the flow valve to close the flow valve and prevent air flow therethrough.

Abstract: A pneumatic excavator configured to be pneumatically actuated includes an actuator; a flow valve fluidly coupled to the actuator an air actuation conduit; and a barrel coupled to an egress of the flow valve, where the barrel defines an outlet of the pneumatic excavator. Actuating the actuator causes compressed air to be transmitted from the actuator through the an air actuation conduit to a first port of the flow valve to open the flow valve and compressed air from a supply of compressed air passes through the flow valve and the outlet of the pneumatic excavator. Releasing the actuator causes the compressed air to be transmitted from the actuator through the at least one air actuation conduit to a second port of the flow valve to cause the flow valve to close and the flow valve prevents the compressed air from the supply of compressed air from passing therethrough.

Abstract: A pneumatic excavator includes: a barrel with an ingress configured to be fluidly connected to a supply of compressed air and an egress; an actuator; a releasable coupling to lock the actuator to the barrel in a plurality positions; and a flow valve fixedly arranged to the barrel, the flow valve in a communicative coupling with the actuator by an actuation conduit. The actuation conduit is flexible and slaved by an adjustment movement of the releasable coupling and actuator along the barrel to thereby maintain the communicative coupling therebetween. When the actuator is actuated, the actuation conduit sends causes the flow valve to open and the compressed air passes through the flow valve and exits the pneumatic excavator, and when the actuator is released, the actuation conduit sends a signal to the flow valve to close to prevent the compressed air from passing through the flow valve.

Abstract: A pneumatic excavator for delivering pulsed compressed air includes an actuator; a controller valve; a flow valve; a barrel defining an outlet of the excavator; and a pulse control line extending between the controller valve and a port downstream from an egress of the flow valve. As compressed air flows through the egress of the flow valve, the pulse control line is pressurized and shifts the controller valve to an actuated position, causing the compressed air from the actuator to close the flow valve, thus preventing the air flow from passing through a primary flow passage and through the outlet. The pulse control line being no longer pressurized by the air flow, then causes the controller valve to move to an unactuated position to cause compressed air from the actuator open the flow valve and permit the air flow through the outlet and again pressurize the pulse control line.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: A fluid dilution control system includes a processor and a plurality of sensors communicatively coupled to the processor. Each of the plurality of sensors is configured to sense a tracer component in a mixed solution of solution and motive fluid, where the tracer component is present in a pre-defined amount in the solution prior to being mixed with the motive fluid in the mixed solution. Each of the plurality of sensors senses a level of the tracer component present in the mixed solution and transmits the sensed information to the processor such that the processor compares the sensed level of each tracer component to a target level of a respective tracer component and causes a rate of dilution of one or more solutions containing the sensed tracer component to be adjusted to reach the target level of the respective tracer component.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: An apparatus for cutting a portion of an immobilization cast to facilitate removal of the cast from a body part of a patient may comprise a handle structure for being held by the hand of a user, a cutting device extending from the handle for cutting the cast material, with the cutting device including a blade and a blade movement device configured to cause ultrasonic movement of the blade, and a shielding structure configured for at least partially positioning between the cast and a part of the patient's body part such that a portion of the shield extends between the blade and the body part to shield the body part from the blade.

Abstract: An apparatus for cutting a portion of an immobilization cast to facilitate removal of the cast from a body part of a patient may comprise a handle structure for being held by the hand of a user, a cutting device extending from the handle for cutting the cast material, with the cutting device including a blade and a blade movement device configured to cause ultrasonic movement of the blade, and a shielding structure configured for at least partially positioning between the cast and a part of the patient's body part such that a portion of the shield extends between the blade and the body part to shield the body part from the blade.