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FDA 510(k) Applications Submitted by STEVE CLARKE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K972436
06/30/1997
T1 LINE DENTAL HANDPIECES
SIEMENS AG
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.
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