Medical Device Manufacturer · US , Ann Arbor , MI

Danmar Products, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2001

Total

Cleared

Denied

Danmar Products, Inc. has 3 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.

Historical record: 3 cleared submissions from 2001 to 2010. Primary specialty: Neurology.

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

Danmar Products, 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 - Danmar Products, Inc.

3 devices

1-3 of 3