Medical Device Manufacturer · US , Crofton , MD

Dermeo - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2010

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared May 21, 2010

MEDIFLASH AND ESTEFLASH

General & Plastic Surgery · 226d