Medical Device Manufacturer · US , Walnut Creek , CA

Acorn Group, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1990

4

Total

4

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Oct 30, 1990

General & Plastic Surgery · 54d

Cleared Jun 05, 1990

IRRIGATION AND SUCTION APPARATUS

General & Plastic Surgery · 126d