Keller Medical Specialties Products, Inc.

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

Keller Medical Specialties Products, Inc. has submitted 6 FDA 510(k) premarket notifications since 1990, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Oximeter, Pacemaker, Cardiac, External Transcutaneous (non-invasive), Alarm, Blood-pressure, Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm), System, Measurement, Blood-pressure, Non-invasive . Use the specialty filter in the sidebar to narrow results.