Kinsei Shiatsu, Inc.

Kinsei Shiatsu, Inc. — FDA 510(k) Submissions

Kinsei Shiatsu, Inc. has submitted 6 FDA 510(k) premarket notifications since 1995, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Massager, Therapeutic, Electric, Vibrator, Therapeutic . Use the specialty filter in the sidebar to narrow results.