Tpl-Cordis, Inc.

Tpl-Cordis, Inc. — FDA 510(k) Submissions

Tpl-Cordis, Inc. has submitted 6 FDA 510(k) premarket notifications since 1987, of which 6 received clearance as substantially equivalent to a predicate device.

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