Cordis Corp.
Cordis Corp. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2014.
Clearances by Cordis Corp. — page 4
301–315 of 315- K781237 — KIDNEY, ARTIFICIAL, C-DAK 2.0
- K781238 — KIDNEY, ARTIFICIAL, C-DAK 1.5
- K781058 — C-DAK 4000 ARTIFICIAL KIDNEY
- K780453 — STANICOR THETA MODEL 221 CARDIAC PACER
- K780066 — CARDIAC PACER, MODEL 208
- K772355 — BLOOD LINE COMP. NEG. PRESS. PILLOW
- K772063 — CATHETER, INTRACRANIAL PRESS. MONITOR.
- K771855 — OMNICOR PROGRAMMER MODEL 222A
- K771529 — PERITONEAL INTRODUCER & SHEATH
- K770951 — CARDIAC PACERS W/NARROW PULSE WIDTH
- K770535 — C-DAK 3500
- K770478 — ADAPTER, CORDIS
- K770214 — TEMP. PERVENOUS LEAD W/REMOTE ANODE
- K761007 — ARTIFICIAL KIDNEY, C-DAK CORDIS DOW
- K760013 — PACER SYSTEMS ANALYZER (CORDIS)
Data sourced from openFDA. This site is unofficial and independent of the FDA.