Medical Device Manufacturer · US , Boise , ID

Oakport Intl., Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Oakport Intl., Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared May 07, 1985

SUNTANNING EQUIPMENT

General & Plastic Surgery · 21d