Cordis Corp. - FDA 510(k) Cleared Devices

Cleared Jul 08, 1980

BIONICS BI-FLO SAFE(DOUBLE LUMEN CATHET

K801356 · KOC

Gastroenterology & Urology · 29d

Cleared May 08, 1980

C-DAK TM 2800 ARTIFICIAL KIDNEY

K800704 · FJI

Gastroenterology & Urology · 38d

Cleared Jan 16, 1980

C-DAK 2100 ARTIFICIAL KIDNEY

K792419 · FJI

Gastroenterology & Urology · 50d

Cleared Mar 21, 1979

A.V. FISTULA NEEDLE SET

K782021 · FIE

Gastroenterology & Urology · 106d

Cleared Feb 22, 1979

ARTIFICIAL KIDNEY, C-DAK 0.6D

K782151 · FJI

Gastroenterology & Urology · 58d

Cleared Jan 17, 1979

DIALYSATE DELIVERY SYSTEM

K781886 · FKP

Gastroenterology & Urology · 71d

Cleared Aug 23, 1978

C-DAK 4000 ARTIFICIAL KIDNEY

K781058 · FJI

Gastroenterology & Urology · 61d

Cleared Jan 26, 1978

BLOOD LINE COMP. NEG. PRESS. PILLOW

K772355 · FIW

Gastroenterology & Urology · 30d

Cleared Apr 15, 1977

C-DAK 3500

K770535 · FIG

Gastroenterology & Urology · 25d

Cleared Jan 12, 1977

ARTIFICIAL KIDNEY, C-DAK CORDIS DOW

K761007 · FJI

Gastroenterology & Urology · 65d