Metronic, Inc.

Metronic, Inc. — FDA 510(k) Submissions

Metronic, Inc. has submitted 4 FDA 510(k) premarket notifications since 1983, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Permanent Pacemaker Electrode, Camera, Scintillation (gamma), Exerciser, Powered, Pacemaker Lead Adaptor . Use the specialty filter in the sidebar to narrow results.