Intermedics, Inc.

Intermedics, Inc. — FDA 510(k) Submissions

Intermedics, Inc. has submitted 211 FDA 510(k) premarket notifications since 1977, of which 201 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Permanent Pacemaker Electrode, Implantable Pacemaker Pulse-generator, Pacemaker Lead Adaptor, Pump, Infusion, Transmitters And Receivers, Electrocardiograph, Telephone . Use the specialty filter in the sidebar to narrow results.