Stryker Physio-Control

Stryker Physio-Control — FDA 510(k) Submissions

Stryker Physio-Control has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Auxiliary Power Supply (ac Or Dc) For Low-energy Dc-defibrillator, Cable, Transducer And Electrode, Patient, (including Connector) . Use the specialty filter in the sidebar to narrow results.