FDA 510(k) Applications Submitted by AMPLIFE CORPORATION

FDA 510(k) Number	Submission Date	Device Name	Applicant
K043550	12/23/2004	AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100	AMPLIFE CORPORATION
K050413	02/18/2005	AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600	AMPLIFE CORPORATION
K042575	09/22/2004	AMPLIFE DIGITAL CLINICAL THERMOMETER	AMPLIFE CORPORATION
K042906	10/21/2004	AMPLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL E101	AMPLIFE CORPORATION