Cordis Corp. - FDA 510(k) Cleared Devices
315
Total
281
Cleared
0
Denied
194 devices
Cleared
Aug 20, 1980
CORDIS FLOW DIRECTED BALLOON CATHETER
Cardiovascular
15d
Cleared
Jul 08, 1980
MULTICOR (GAMMA) MODEL 336 & MODEL 337
Cardiovascular
60d
Cleared
Dec 05, 1979
STANICOR, OMNI-STAN,MOD 333B,334A GAMMA
Cardiovascular
16d
Cleared
Nov 27, 1979
OMNICOR PROGRAMMER MODEL 222C
Cardiovascular
133d
Cleared
Nov 05, 1979
CORDIS PERMANENT PERVENOUS CARDIAC LEADS
Cardiovascular
61d
Cleared
Oct 22, 1979
OMNI-STANICOR (THETA) MOD 237A
Cardiovascular
41d
Cleared
Sep 28, 1979
CORDIS BIPOLAR PACER CONNECTOR SYSTEM
Cardiovascular
16d
Cleared
Jul 24, 1979
PERVENOUS LEAD INTRODUCER SYSTEM
Cardiovascular
15d
Cleared
May 16, 1979
OMNI-STANICOR-(THETA) MODEL 217
Cardiovascular
36d
Cleared
Apr 17, 1979
BIPOLAR PERNENOUS VENTRICULAR LEAD
Cardiovascular
55d
Cleared
Feb 23, 1979
MOVABLE CORE SAFETY GUIDE
Cardiovascular
17d
Cleared
Feb 08, 1979
BIPOLAR, STANICOR LAMBDA MODEL 236,235
Cardiovascular
36d
Cleared
Jun 30, 1978
STANICOR THETA MODEL 221 CARDIAC PACER
Cardiovascular
102d
Cleared
Jan 30, 1978
CARDIAC PACER, MODEL 208
Cardiovascular
18d
Cleared
Oct 07, 1977
OMNICOR PROGRAMMER MODEL 222A
Cardiovascular
9d
Cleared
Jun 20, 1977
CARDIAC PACERS W/NARROW PULSE WIDTH
Cardiovascular
26d
Cleared
Mar 30, 1977
ADAPTER, CORDIS
Cardiovascular
19d
Cleared
Mar 28, 1977
TEMP. PERVENOUS LEAD W/REMOTE ANODE
Cardiovascular
54d
Cleared
Jul 20, 1976
PACER SYSTEMS ANALYZER (CORDIS)
Cardiovascular
40d
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