Medical Device Manufacturer · US , Washington , DC

Prestige Medical Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

Recent clearances: PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Prestige Medical Corp. General Hospital ✕

1 devices

1-1 of 1

Cleared Mar 03, 1998

PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE

General Hospital · 586d