Rabar, Inc.

Rabar, Inc. — FDA 510(k) Submissions

Rabar, Inc. has submitted 3 FDA 510(k) premarket notifications since 1982, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Nerve, Transcutaneous, For Pain Relief, Mallet, Surgical, General & Plastic Surgery, Echoencephalograph . Use the specialty filter in the sidebar to narrow results.