Abstract: An apparatus and method for delivering fluid from a syringe to a subject using a pumping device of a flow control apparatus. The method includes locating the flow control apparatus on a horizontal support surface. Providing the syringe with a volume of fluid including a total amount of preferred nutrient and an amount of non-preferred nutrient liquid. Mounting the syringe relative to the flow control apparatus whereby the syringe is oriented in a generally vertical orientation such that an outlet of the syringe faces upward. Initiating operation of the pumping device to draw the fluid from the syringe for a duration of time to preferentially deliver at least a portion of the total amount of preferred nutrient in the fluid to the subject.

Abstract: A single device is provided for performing hysterography and intrauterine venography having a marker that aids in positioning the device within the patient, having a bulb-tip to seal the cervix, having a bulb-tip opening to allow an image enhancing medium to be discharged from a needle and injected into the uterus to perform the hysterography, having a needle to discharge and inject an image enhancing medium into the fundal myometrium to perform the intrauterine venography, and having a needle securing mechanism to secure the needle to prevent patient injury during transcervical introduction of the device.

Abstract: A device and method for delivering a bioactive to the uterine wall. In one embodiment, the device comprises a balloon having the bioactive present within the material of the balloon or on an outside surface of the balloon. Another embodiment provides a method comprising inserting the balloon into the uterus, inflating the balloon so that the outside surface of the balloon exerts pressure on uterine wall and delivering the bioactive to the uterine wall.

Abstract: An implantable medical device comprising an inner region and an outer region positioned over at least a portion of the inner region and in contact with a surface of the inner region. The durometer of the inner region is greater than the durometer of the outer region and a pharmacologically active ingredient is present in at least a portion of the inner region or the outer region.