Catheter Research, Inc.

Catheter Research, Inc. — FDA 510(k) Submissions

Catheter Research, Inc. has submitted 8 FDA 510(k) premarket notifications since 1994, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cannula, Manipulator/injector, Uterine, Stethoscope, Esophageal, With Electrical Conductors, Catheter, Assisted Reproduction, Analyzer, Gas, Carbon-dioxide, Gaseous-phase, Connector, Airway (extension) . Use the specialty filter in the sidebar to narrow results.