Promedtek, Inc.

Promedtek, Inc. — FDA 510(k) Submissions

Promedtek, Inc. has submitted 2 FDA 510(k) premarket notifications since 2007, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat, Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat . Use the specialty filter in the sidebar to narrow results.