Medical Device Manufacturer · US , Southbridge , MA

Henke Sass Wolf of America, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1994

9

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Henke Sass Wolf of America, Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared Oct 30, 1998

General Hospital · 58d