Medical Device Manufacturer · US , Washington , DC

Kavo America - FDA 510(k) Cleared Devices

20 submissions · 19 cleared · Since 1991

20

Total

19

Cleared

1

Denied

FDA 510(k) Regulatory Record - Kavo America General Hospital ✕

1 devices

1-1 of 1

Cleared Aug 26, 1991

KAVOKLAVE STEAM AUTOCLAVE

General Hospital · 182d