Sentry Medical Products, Inc.

Sentry Medical Products, Inc. — FDA 510(k) Submissions

Sentry Medical Products, Inc. has submitted 13 FDA 510(k) premarket notifications since 1983, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrode, Electrocardiograph, Electrode, Cutaneous, Cable, Transducer And Electrode, Patient, (including Connector), Catheter, Umbilical Artery, Electrode, Electrosurgical . Use the specialty filter in the sidebar to narrow results.