Siemens Elema AB - FDA 510(k) Cleared Devices
63
Total
60
Cleared
0
Denied
Siemens Elema AB has 60 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 60 cleared submissions from 1978 to 2003. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Siemens Elema AB Filter by specialty or product code using the sidebar.
63 devices
Cleared
Sep 05, 2003
COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81E
Anesthesiology
333d
Cleared
Jan 23, 2002
KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392E
Cardiovascular
302d
Cleared
Dec 18, 2001
SERVOI VENTILATOR SYSTEM, MODEL 64 87 800 E407E
Anesthesiology
266d
Cleared
Oct 05, 2000
CATHCOR DESKTOP
Cardiovascular
83d
Cleared
May 26, 2000
MODIFICATION TO KION ANESTHESIA SYSTEM
Anesthesiology
30d
Cleared
Oct 14, 1997
SERVO VENTILATOR 300A
Anesthesiology
221d
Cleared
Oct 25, 1996
SERVO VENTILATOR 300 COMPUTER INTERFACE
Anesthesiology
297d
Cleared
Oct 25, 1996
SIEMENS SERVO SCREEN 390 AND SERVO COMPUTER MODULE 990
Anesthesiology
283d
Cleared
Sep 03, 1987
SIEMENS O2-AIR MIXER 965
Anesthesiology
80d
Cleared
Jul 21, 1987
SERVO VENTILATOR 900 C/D
Anesthesiology
106d
Cleared
Jun 15, 1987
SIEMENS DRY AIR COMPRESSOR
Anesthesiology
35d
Cleared
May 14, 1987
SIEMENS MAIN FLOW BACTERIA FILTER
General Hospital
37d
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