Cordis Corp.
Cordis Corp. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2014.
Clearances by Cordis Corp. — page 3
201–300 of 315- K855126 — CORDIS CATHETER SHEATH INTRODUCERS,STERI-SLEEVES
- K851968 — CORDIS MULTICOR ST, MODEL 350A
- K855058 — EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID
- K854657 — INTRACRANIAL PRESSURE MONITORING CUP CATHETERS
- K854214 — MULTICOR II 402B & 402C MULTIPROGRAM. CARDIAC PACE
- K854474 — EXTERNAL VENTRICULAR DRAINAGE/MONITORING/LUMBAR SE
- K852748 — CORDIS MODELS 336A,336B,337A & 334 CARDIAC PACEMAK
- K851913 — CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA
- K844913 — CORDIS PTA CATHETER-PERCUTANEOUS CATHETER
- K851947 — PTCA GUIDING CATHETER
- K852827 — CORDIS EXTERNAL NEURAL STIMULATOR MODEL 911A
- K852253 — 329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR
- K850329 — CORDIA S4 -TREPONEMA PALLIDUM
- K851420 — MULTICOR S, MODELS 330A/331A
- K844360 — CORDIS MULTICOR S 330A & 331A CARDIAC PACEMAKERS
- K844815 — CORDIS ELECTROPHYSIOLOGY STIMULATOR
- K851416 — STANICOR GAMMA 333B/334A
- K851417 — MULTICOR GAMMA MODELS 336/337
- K851418 — OMNI-ATRICOR MODEL 308A
- K851419 — MULTICOR GAMMA 402 SERIES PACER
- K844969 — CORDIS DUAL-CHAMBER PSA MODEL 296A (PACEMAKER)
- K843751 — CORDIA HS ANTIBODY TYPING REAGENTS
- K844970 — CORDIS ENCOR PERVENOUS ATRIAL & VENTRICULAR LEADS
- K844294 — CORDIA IC
- K843417 — CORDIA T-M
- K844161 — PTCA GUIDING CATHER
- K811259 — CORDIS ENCOR ATRIAL LEAD
- K834416 — LUMELEC ELECTRODE CATHETER
- K834548 — HYPODERMIC SYRINGES & NEEDLES
- K833078 — HOLLOW FIBER MEMBRANE OXYGENATOR-HF4000
- K834107 — ANGIOPLASTY INFLATION DEVICE & CARTR
- K832875 — CORDIA HS
- K832561 — EPCOR MULTIELECTRODE TEMP. PERVENOUS
- K831105 — CORDIA PAP
- K830729 — C-DAK ARTIFICIAL KIDNEY
- K823761 — ERYTHROCYTE & STAND SEDIMENT. RATE TUBE
- K823763 — VARIOUS-SPECIMEN COLLECTORS
- K823760 — PRICK-TEST NEEDLE
- K823762 — VARIOUS-ANALYZER CUPS
- K823123 — CORDIA CMV
- K823530 — STIMUCORD EXTERNAL NEURAL STIM. 911A
- K821889 — POROUS SURFACED PLATINUM IRIDIUM
- K821489 — CORDIA TG
- K820356 — MULTICOR (GAMMA) 402 CARDIAC PACER
- K812781 — TEMPORARY PERVENOUS J-ATRIAL LEAD
- K812540 — CORDIA IM
- K811830 — C-DAK DUO-FLUX ARTIFICIAL KIDNEY
- K812242 — CORDISNHYPERION HEMOGLOBIN A1 TEST SYS
- K812168 — CORDIS DUCOR PERCUT. TRANS. ANGIO. CATH.
- K812231 — INTRAVENOUS ADMINISTRATION SET
- K811971 — CORDIS DUCOR PTR SYSTEM
- K811892 — CORDIS DOW SERA FLO TM TRANSDUCER PROT
- K811691 — CORDIS OMNI-ARTICOR CARDIAC PACER #308
- K811539 — CORDIS ENCOR PEWENOUS VENTRICULAR BIPOL
- K810999 — CORDIS TCPO2 TRANCUTANEOUS OXYGEN PRESS
- K810849 — CORDIS BIOPSY FORCEPS
- K810315 — ALTERNATE STERILIZ. FOR CELLULOSE ACET
- K810552 — CORDIS PACEMAKER PROGRAMMERS 255A & 256A
- K810432 — CORDIS PERVENOUS ATRIAL LEAD
- K810046 — CORDIA A
- K802894 — CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY
- K810319 — CORDIS STIMUCORD EXTERNAL NEUTRAL STIM
- K802893 — CORDIS DOW C-DAK 1.3MRC ARTIF. KIDNEY
- K810041 — CORDIS TEMPORATY CURVED ATRIAL LEAD
- K810202 — CORDIS MULTIFILAR PERVENOUS VENTRIC. LD
- K803258 — CORDIS HAKIM ASCITES VALVE SYSTEM
- K802613 — C-PAK MODEL 12 ARTIFICIAL KIDNEY
- K802221 — CHRONOCOR IV MODEL 250
- K802629 — STERI-SLEEVE
- K802301 — CORDIS DOW INFUSION PUMP
- K802338 — TORQUE CONTROL BALLOON CATHETER
- K801910 — INSULATING SHEATH
- K801865 — CORDIS FLOW DIRECTED BALLOON CATHETER
- K801731 — C-DAK DUO-FLUX ARTIFICIAL KIDNEY
- K801106 — MULTICOR (GAMMA) MODEL 336 & MODEL 337
- K801354 — BIONICS ARTERIAL/VENOUS FISTULA NEEDLE
- K801355 — BIONICS BI-FLO STRETCH(DOUBLE LUMEN FOR
- K801356 — BIONICS BI-FLO SAFE(DOUBLE LUMEN CATHET
- K800704 — C-DAK TM 2800 ARTIFICIAL KIDNEY
- K800991 — CORDIA N
- K800992 — CORDIA NP
- K800074 — VESSEL OCCLUDER
- K792419 — C-DAK 2100 ARTIFICIAL KIDNEY
- K792348 — STANICOR, OMNI-STAN,MOD 333B,334A GAMMA
- K791419 — OMNICOR PROGRAMMER MODEL 222C
- K792061 — CORDIA RF
- K791768 — CORDIS PERMANENT PERVENOUS CARDIAC LEADS
- K791783 — OMNI-STANICOR (THETA) MOD 237A
- K791784 — CORDIS BIPOLAR PACER CONNECTOR SYSTEM
- K791276 — PERVENOUS LEAD INTRODUCER SYSTEM
- K790690 — OMNI-STANICOR-(THETA) MODEL 217
- K790344 — BIPOLAR PERNENOUS VENTRICULAR LEAD
- K790212 — CORDIA T
- K782021 — A.V. FISTULA NEEDLE SET
- K790258 — MOVABLE CORE SAFETY GUIDE
- K782151 — ARTIFICIAL KIDNEY, C-DAK 0.6D
- K790014 — BIPOLAR, STANICOR LAMBDA MODEL 236,235
- K790010 — MANIFOLD, DISPOSABLE 3 VALVE
- K780885 — CORDIA R
- K781886 — DIALYSATE DELIVERY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.