Datex Division Instrumentarium Corp. - FDA 510(k) Cleared Devices
55
Total
55
Cleared
0
Denied
Datex Division Instrumentarium Corp. has 55 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 55 cleared submissions from 1982 to 1997. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Datex Division Instrumentarium Corp. Filter by specialty or product code using the sidebar.
55 devices
Cleared
Feb 06, 1997
AS/3 ESTPR MODULE
Cardiovascular
580d
Cleared
Oct 23, 1996
AS/3 LIGHT MONITOR
Cardiovascular
205d
Cleared
Feb 14, 1995
AS/3 AIRWAY MODULE
Anesthesiology
211d
Cleared
Jan 27, 1995
AS/3 MEMORY MODULE, M0MEM
Anesthesiology
92d
Cleared
Dec 30, 1994
DATEX AS/3 PATIENT MONITOR
Cardiovascular
549d
Cleared
Nov 14, 1994
DATEX AS/3 TM ANAESTHESIA MONITOR
Anesthesiology
496d
Cleared
Oct 17, 1994
AS/3 NELLCOR COMPATIBLE SATURATION MOODULE, M-NSAT
Anesthesiology
91d
Cleared
Aug 09, 1994
ANAESTHESIA RECORD KEEPER
Anesthesiology
771d
Cleared
Aug 01, 1994
AS/3(TM) ANESTHESIA MONITOR SYST INTERFACE BOARD
Anesthesiology
259d
Cleared
Jul 27, 1994
AS/3 PRESSURE TEMPERATURE MODULE, M-PT
Cardiovascular
9d
Cleared
Jul 11, 1994
AS/3 TM NETWORK
Anesthesiology
370d
Cleared
Nov 29, 1993
CAPNOMAC ULTIMA ANESTHESIA MONITOR
Anesthesiology
210d
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