Abstract: An apparatus comprising a first light source, a second light source, a controller and a power source. The first light source may activate color channels of a reactive material in response to a signal. The second light source may deactivate a subset of the color channels of the reactive material in response to the signal. The controller may receive an input, determine characteristics for the light sources in response to the input and generate the signal in response to the first characteristics and the second characteristics. The power source may provide power for the light sources and the controller. The reactive material may change appearance in response to the subset of the color channels deactivated. The power source and the controller may be contained in a housing of the apparatus. The light sources may enable the apparatus to emit light onto an object comprising the reactive material.

Abstract: An apparatus includes a container, a plurality of lights and a circuit. The container may comprise an outer shell comprising a material configured to protect contents of the apparatus and an inner surface. The outer shell may be configured to open to enable the contents to be placed on the inner surface. A cavity may be formed within the container when the outer shell is closed. The plurality of lights implemented on the inner surface may each be configured to adjust a characteristic of light output in response to a signal. The circuit may be configured to generate the signal in response to an input. The circuit may be implemented between the outer shell and the inner surface. A reactive material of the contents of the container may be configured to change appearance in response to the characteristic of light.

Abstract: An apparatus includes a container, a plurality of lights and a circuit. The container may comprise an outer shell comprising a material configured to protect contents of the apparatus and an inner surface. The outer shell may be configured to open to enable the contents to be placed on the inner surface. A cavity may be formed within the container when the outer shell is closed. The plurality of lights implemented on the inner surface may each be configured to adjust a characteristic of light output in response to a signal. The circuit may be configured to generate the signal in response to an input. The circuit may be implemented between the outer shell and the inner surface. A reactive material of the contents of the container may be configured to change appearance in response to the characteristic of light.

Abstract: The present invention relates to a buckle system including a male subassembly and female subassembly that are designed to mate with one another. The male subassembly also includes a printed circuit board (PCB) that may mate with an electrical connector within the female subassembly, thus completing a circuit for providing power to an electronic device when the subassemblies are mated. The male subassembly is connected to a cable portion that, when pulled with sufficient force, causes the male subassembly and its PCB to disengage the female subassembly and its electrical connector. The PCB and electrical connector may also be connected within standard side-release male and female subassemblies, respectively, for use in standard side-release buckles.

Abstract: Disclosed is a disposable patient interface for an intraductal fluid aspiration system. The interface has a flexible tubular distal member for contacting the patient, and a proximal support portion forming a vacuum chamber therein. The support portion has a vacuum aperture for communication with a source of vacuum, and a retention structure for releasably mounting within a hand piece of an intraductal fluid aspiration system. The flexible member preferably has a low modulus of elasticity and a high tear strength, such that it can be stretched to fit over a rigid support without rupture.

Abstract: The present invention relates to a buckle system including a male subassembly and female subassembly that are designed to mate with one another. The male subassembly also includes a printed circuit board (PCB) that may mate with an electrical connector within the female subassembly, thus completing a circuit for providing power to an electronic device when the subassemblies are mated. The male subassembly is connected to a cable portion that, when pulled with sufficient force, causes the male subassembly and its PCB to disengage the female subassembly and its electrical connector. The PCB and electrical connector may also be connected within standard side-release male and female subassemblies, respectively, for use in standard side-release buckles.

Abstract: Disclosed is a disposable patient interface for an intraductal fluid aspiration system. The interface has a flexible tubular distal member for contacting the patient, and a proximal support portion forming a vacuum chamber therein. The support portion has a vacuum aperture for communication with a source of vacuum, and a retention structure for releasably mounting within a hand piece of an intraductal fluid aspiration system. The flexible member preferably has a low modulus of elasticity and a high tear strength, such that it can be stretched to fit over a rigid support without rupture.

Abstract: Disclosed is a disposable patient interface for an intraductal fluid aspiration system. The interface has a flexible tubular distal member for contacting the patient, and a proximal support portion forming a vacuum chamber therein. The support portion has a vacuum aperture for communication with a source of vacuum, and a retention structure for releasably mounting within a hand piece of an intraductal fluid aspiration system. The flexible member preferably has a low modulus of elasticity and a high tear strength, such that it can be stretched to fit over a rigid support without rupture.

Abstract: Disclosed is a disposable closed fluid loop for providing heat and compression to an intraductal fluid aspiration device. A plurality of bladders are configured to receive a pressurized inflation fluid, and to inflate in response thereto. The fluid is further configured to flow adjacent a heat exchanger, thereby receiving thermal energy, which it imparts to the bladders through conduction. Accordingly, the disclosed fluid loop provides heated inflation media to inflate a plurality of bladders to provide heat and compression to an intraductal fluid aspiration patient.

Abstract: Disclosed is a method and apparatus for accomplishing a noninvasive screen for breast disease markers, including breast cancer markers and cytologically abnormal cells. Intraductal fluid is noninvasively aspirated using compression, heating and suction cycles. The removed sample is thereafter assayed for the presence of cytologically abnormal cells and/or one or more breast disease markers. In addition to the diagnostic applications of the disclosed method and apparatus, a therapeutic application is also contemplated wherein intraductal fluids are noninvasively aspirated using compression, heating and suction cycles to remove toxic buildups within the fluid.

Abstract: Disclosed is a method and apparatus for accomplishing a noninvasive screen for breast disease markers, including breast cancer markers and cytologically abnormal cells. Intraductal fluid is noninvasively aspirated using compression, heating and suction cycles. The removed sample is thereafter assayed for the presence of cytologically abnormal cells and/or one or more breast disease markers. In addition to the diagnostic applications of the disclosed method and apparatus, a therapeutic application is also contemplated wherein intraductal fluids are noninvasively aspirated using compression, heating and suction cycles to remove toxic buildups within the fluid.

Abstract: Disclosed is a disposable patient interface for an intraductal fluid aspiration system. The interface has a flexible tubular distal member for contacting the patient, and a proximal support portion forming a vacuum chamber therein. The support portion has a vacuum aperture for communication with a source of vacuum, and a retention structure for releasably mounting within a hand piece of an intraductal fluid aspiration system. The flexible member preferably has a low modulus of elasticity and a high tear strength, such that it can be stretched to fit over a rigid support without rupture.

Abstract: Disclosed is an apparatus for noninvasive intraductal fluid aspiration. Intraductal fluid is noninvasively aspirated using compression, heating and suction cycles. The device is configured to provide a compression force, deliver heat, and apply a vacuum pressure to encourage the aspiration of patient fluid. The device includes an adjustable support and a movable wall for applying compression. Withdrawn fluid may be used either for diagnostic or therapeutic purposes.

Abstract: Disclosed is a method and apparatus for accomplishing a noninvasive screen for breast disease markers, including breast cancer markers and cytologically abnormal cells. Intraductal fluid is noninvasively aspirated using compression, heating and suction cycles. The removed sample is thereafter assayed for the presence of cytologically abnormal cells and/or one or more breast disease markers. In addition to the diagnostic applications of the disclosed method and apparatus, a therapeutic application is also contemplated wherein intraductal fluids are noninvasively aspirated using compression, heating and suction cycles to remove toxic buildups within the fluid.

Abstract: A method is disclosed for noninvasively obtaining intraductal fluid. The method includes the use of an intraductal fluid sampling device to contact the patient, provide compression, and deliver heat thereto according to predetermined cycle characteristics. The cycle characteristics, such as compression cycle times and compression rates, may be varied and controlled by a control circuit.

Abstract: Disclosed is a method and apparatus for accomplishing a noninvasive screen for breast disease markers, including breast cancer markers and cytologically abnormal cells. Intraductal fluid is noninvasively aspirated using compression, heating and suction cycles. The removed sample is thereafter assayed for the presence of cytologically abnormal cells and/or one or more breast disease markers. In addition to the diagnostic applications of the disclosed method and apparatus, a therapeutic application is also contemplated wherein intraductal fluids are noninvasively aspirated using compression, heating and suction cycles to remove toxic buildups within the fluid.

Abstract: A method is disclosed for noninvasively obtaining intraductal fluid. The method includes the use of an intraductal fluid sampling device to contact the patient, provide compression, and deliver heat thereto according to predetermined cycle characteristics. The cycle characteristics, such as compression cycle times and compression rates, may be varied and controlled by a control circuit.

Abstract: A method is disclosed for noninvasively obtaining intraductal fluid. The method includes the use of an intraductal fluid sampling device to contact the patient, provide compression, and deliver heat thereto according to predetermined cycle characteristics. The cycle characteristics, such as compression cycle times and compression rates, may be varied and controlled by a control circuit.

Abstract: Disclosed is a disposable patient interface for an intraductal fluid aspiration system. The interface has a flexible tubular distal member for contacting the patient, and a rigid proximal member forming a vacuum chamber therein. The rigid member has a vacuum aperture for communication with a source of vacuum. The flexible member preferably has a low modulus of elasticity and a high tear strength, such that it can be stretched to fit over a rigid support without rupture.