Medical Device Manufacturer · US , Mchenry , IL

Edward Weck, Inc. - FDA 510(k) Cleared Devices

140 submissions · 140 cleared · Since 1976

140

Total

140

Cleared

0

Denied

FDA 510(k) Regulatory Record - Edward Weck, Inc. General Hospital ✕

3 devices

1-3 of 3

Cleared Feb 15, 1990

BOWIE-DICK TEST CARD CATALOG NUMBER 008018

General Hospital · 58d

Cleared Jan 28, 1980

STERILIZING CASE CAT. NO. 65199

General Hospital · 14d

Cleared Apr 05, 1978

General Hospital · 99d