Medical Device Manufacturer · US , Washington, Dc , DC

Perfaction, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2009

Recent clearances: AIRGENT, MODEL AG7000010

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Jan 23, 2009

AIRGENT, MODEL AG7000010

General Hospital · 178d