Medical Device Manufacturer · US , Indianapolis , IN

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

3 submissions · 3 cleared · Since 2010

Total

Cleared

Denied

Sonarmed, Inc. has 3 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Historical record: 3 cleared submissions from 2010 to 2020. Primary specialty: Anesthesiology.

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

Sonarmed, 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 - Sonarmed, Inc.

3 devices

1-3 of 3