Medical Device Manufacturer · US , Lilburn , GA

Accu-Path - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1990

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Accu-Path General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Oct 30, 1990

ACCU PATH STERILE LABEL

General & Plastic Surgery · 20d