Midmark Corporation

Midmark Corporation — FDA 510(k) Submissions

Midmark Corporation has submitted 5 FDA 510(k) premarket notifications since 2016, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Sterilizer, Steam, Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms), X-ray, Tomography, Computed, Dental, Unit, Operative Dental . Use the specialty filter in the sidebar to narrow results.