Critikon Company, LLC - FDA 510(k) Cleared Devices
51
Total
51
Cleared
0
Denied
Critikon Company, LLC has 51 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 51 cleared submissions from 1979 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Critikon Company, LLC Filter by specialty or product code using the sidebar.
51 devices
Cleared
Sep 21, 2000
DINAMAP PRO 1000 MONITOR, MODEL 1000
Cardiovascular
58d
Cleared
May 26, 2000
DINAMAP ADVANCED NIBP MODULE
Cardiovascular
102d
Cleared
Feb 24, 2000
DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400
Cardiovascular
202d
Cleared
Aug 14, 1998
DINAMAP MPS SELECT PORTABLE MONITOR
Cardiovascular
39d
Cleared
Jun 16, 1995
DINAMAP PLUS VITAL SIGNS MONOITOR
Cardiovascular
319d
Cleared
Mar 01, 1995
DINAMAP VITAL SIGNS MONITOR MODELS 9300 AND 9320/9340
Cardiovascular
266d
Cleared
Feb 09, 1994
CRITIKON CENTRAL STATIN MONITOR
Cardiovascular
212d
Cleared
Dec 14, 1993
CHANGES TO PROTECTIV(TM) & JELCO(TM) WINGED CATH
General Hospital
208d
Cleared
Jul 01, 1993
CRITIKON VITAL SIGNS MODULE
Cardiovascular
556d
Cleared
May 17, 1993
INTRAVENOUS CATHETERS MODIFICATIONS
Gastroenterology & Urology
431d
Cleared
Dec 04, 1991
DINAMAP PLUS PHYSIOLOGICAL MONITOR MODEL 8700
Cardiovascular
201d
Cleared
Jun 03, 1991
RATEMINDER(TM) V INFUSION PUMP, MODIFICATION
General Hospital
45d
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