Cordis Corp. - FDA 510(k) Cleared Devices
315
Total
281
Cleared
0
Denied
315 devices
Cleared
Aug 31, 1978
KIDNEY, ARTIFICIAL, C-DAK 2.0
Toxicology
42d
Cleared
Aug 31, 1978
KIDNEY, ARTIFICIAL, C-DAK 1.5
Toxicology
42d
Cleared
Aug 23, 1978
C-DAK 4000 ARTIFICIAL KIDNEY
Gastroenterology & Urology
61d
Cleared
Jun 30, 1978
STANICOR THETA MODEL 221 CARDIAC PACER
Cardiovascular
102d
Cleared
Jan 30, 1978
CARDIAC PACER, MODEL 208
Cardiovascular
18d
Cleared
Jan 26, 1978
BLOOD LINE COMP. NEG. PRESS. PILLOW
Gastroenterology & Urology
30d
Cleared
Jan 03, 1978
CATHETER, INTRACRANIAL PRESS. MONITOR.
Neurology
62d
Cleared
Oct 07, 1977
OMNICOR PROGRAMMER MODEL 222A
Cardiovascular
9d
Cleared
Aug 16, 1977
PERITONEAL INTRODUCER & SHEATH
Neurology
8d
Cleared
Jun 20, 1977
CARDIAC PACERS W/NARROW PULSE WIDTH
Cardiovascular
26d
Cleared
Apr 15, 1977
C-DAK 3500
Gastroenterology & Urology
25d
Cleared
Mar 30, 1977
ADAPTER, CORDIS
Cardiovascular
19d
Cleared
Mar 28, 1977
TEMP. PERVENOUS LEAD W/REMOTE ANODE
Cardiovascular
54d
Cleared
Jan 12, 1977
ARTIFICIAL KIDNEY, C-DAK CORDIS DOW
Gastroenterology & Urology
65d
Cleared
Jul 20, 1976
PACER SYSTEMS ANALYZER (CORDIS)
Cardiovascular
40d
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