Medical Device Manufacturer · US , Millington , MI

Gunnell, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

Total

Cleared

Denied

Gunnell, Inc. has 1 FDA 510(k) cleared medical devices. Based in Millington, US.

Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Gunnell, Inc. Filter by specialty or product code using the sidebar.

Gunnell, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gunnell, Inc.

1 devices

1-1 of 1