Surnic Corporation

Surnic Corporation — FDA 510(k) Submissions

Surnic Corporation has submitted 2 FDA 510(k) premarket notifications since 2021, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Apparatus, Exhaust, Surgical . Use the specialty filter in the sidebar to narrow results.