FDA 510(k) Applications Submitted by STEVEN A CLARKE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K960010	01/02/1996	SERVO VENTILATOR 300 COMPUTER INTERFACE	SIEMENS ELEMA AB
K960168	01/16/1996	SIEMENS SERVO SCREEN 390 AND SERVO COMPUTER MODULE 990	SIEMENS ELEMA AB
K950264	01/23/1995	MAGLIFE	ODAM
K960854	03/01/1996	SIEMENS SERVO ULTRA NEBULIZER 345	PACESETTER, INC.
K972168	06/09/1997	SIDEXIS DIGITAL RADIOGRAPHY SYSTEM	PELTON & CRANE CO.
K962354	06/18/1996	DIOMED 15, 30, 60 SURGICAL DIODE LASER	LIFESTREAM INT'L, INC.
K972276	06/18/1997	CEREC 2 CROWN SOFTWARE	SIEMENS AG
K972312	06/20/1997	SIEMENS ORTHOPHOS DS/DS CEPH	SIEMENS AG
K972535	07/08/1997	MAGLIFE C	ODAM
K983395	09/25/1998	FETALGARD 3000 FETAL MONITOR	ANALOGIC CORP.
K980411	02/03/1998	NPB3900 SERIES PATIENT MONITORS	ANALOGIC CORP.
K011304	04/30/2001	OB-1 FETAL MONITOR	ANALOGIC CORP.
K002503	08/14/2000	FETALGARD LITE	ANALOGIC CORP.
K973198	08/26/1997	VGF-7 VASCULAR GRAFT FLOWMETER	MEDICARD LTD.
K974420	11/24/1997	M1730B TRACEMASTER ECG SYSTEM, M1766B LOCAL EDIT STATION, M1798B REMOTE EDIT STATION	HEWLETT-PACKARD CO.
K965203	12/26/1996	RADX SYSTEM	ELECTRO MEDICAL SYSTEMS, INC.