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Cordis Corp.

315 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
KIDNEY, ARTIFICIAL, C-DAK 2.0 (K781237)Cordis Corp.1978-08-31
KIDNEY, ARTIFICIAL, C-DAK 1.5 (K781238)Cordis Corp.1978-08-31
C-DAK 4000 ARTIFICIAL KIDNEY (K781058)Cordis Corp.1978-08-23
STANICOR THETA MODEL 221 CARDIAC PACER (K780453)Cordis Corp.1978-06-30
CARDIAC PACER, MODEL 208 (K780066)Cordis Corp.1978-01-30
BLOOD LINE COMP. NEG. PRESS. PILLOW (K772355)Cordis Corp.1978-01-26
CATHETER, INTRACRANIAL PRESS. MONITOR. (K772063)Cordis Corp.1978-01-03
OMNICOR PROGRAMMER MODEL 222A (K771855)Cordis Corp.1977-10-07
PERITONEAL INTRODUCER & SHEATH (K771529)Cordis Corp.1977-08-16
CARDIAC PACERS W/NARROW PULSE WIDTH (K770951)Cordis Corp.1977-06-20
C-DAK 3500 (K770535)Cordis Corp.1977-04-15
ADAPTER, CORDIS (K770478)Cordis Corp.1977-03-30
TEMP. PERVENOUS LEAD W/REMOTE ANODE (K770214)Cordis Corp.1977-03-28
ARTIFICIAL KIDNEY, C-DAK CORDIS DOW (K761007)Cordis Corp.1977-01-12
PACER SYSTEMS ANALYZER (CORDIS) (K760013)Cordis Corp.1976-07-20
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