Telectronics, Inc.

Telectronics, Inc. — FDA 510(k) Submissions

Telectronics, Inc. has submitted 107 FDA 510(k) premarket notifications since 1977, of which 107 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implantable Pacemaker Pulse-generator, Permanent Pacemaker Electrode, Pacemaker Lead Adaptor, Pulse-generator, Pacemaker, External, Introducer, Catheter . Use the specialty filter in the sidebar to narrow results.