Medical Device Manufacturer · US , Mchenry , IL

Cordis Corp. - FDA 510(k) Cleared Devices

315 submissions · 281 cleared · Since 1976

Recent clearances: FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM, POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER, ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE

Official Website

315

Total

281

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cordis Corp. General Hospital ✕

6 devices

1-6 of 6

Cleared May 09, 1995

CORDIS CSF RESERVOIR

General Hospital · 103d

Cleared Mar 06, 1984

HYPODERMIC SYRINGES & NEEDLES

General Hospital · 70d

Cleared Jan 19, 1983

VARIOUS-SPECIMEN COLLECTORS

General Hospital · 36d

Cleared Aug 20, 1981

INTRAVENOUS ADMINISTRATION SET

General Hospital · 9d

Cleared Oct 23, 1980

CORDIS DOW INFUSION PUMP

General Hospital · 31d

Cleared Feb 01, 1979

MANIFOLD, DISPOSABLE 3 VALVE

General Hospital · 30d