Medical Device Manufacturer · US , West Cadwell , NJ

Schiff & Co. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1988

15

Total

15

Cleared

0

Denied

FDA 510(k) Regulatory Record - Schiff & Co. General Hospital ✕

3 devices

1-3 of 3

Cleared Oct 01, 1998

VYGON DOUBLE LUMEN UMBILICAL CATHETER

General Hospital · 147d

Cleared Oct 28, 1996

VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM

General Hospital · 399d

Cleared Feb 14, 1995

VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE

General Hospital · 209d