Medrad, Inc.
Medrad, Inc. — FDA 510(k) Submissions
Medrad, Inc. has submitted 105 FDA 510(k) premarket notifications since 1976, of which 105 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Injector And Syringe, Angiographic, Coil, Magnetic Resonance, Specialty, System, Nuclear Magnetic Resonance Imaging, Pump, Infusion, Catheter, Intravascular, Diagnostic . Use the specialty filter in the sidebar to narrow results.
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