Medical Device Manufacturer · DE , Hoechberg

Carefusion Germany 234 GmbH - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2010

12

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - Carefusion Germany 234 GmbH General Hospital ✕

1 devices

1-1 of 1

Cleared Oct 17, 2011

General Hospital · 151d