Medical Device Manufacturer · US , Washington , DC

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

2 submissions · 2 cleared · Since 2007

Total

Cleared

Denied

Promedtek, Inc. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 2007 to 2016. Primary specialty: Physical Medicine.

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

Promedtek, Inc. is one of 4741 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

2 devices

1-2 of 2