Medi-Tate , Ltd.

Medi-Tate , Ltd. — FDA 510(k) Submissions

Medi-Tate , Ltd. has submitted 2 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Temporarily-placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia . Use the specialty filter in the sidebar to narrow results.