Snowden-Pencer

Snowden-Pencer — FDA 510(k) Submissions

Snowden-Pencer has submitted 10 FDA 510(k) premarket notifications since 1986, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Insufflator, Laparoscopic, Laparoscope, General & Plastic Surgery, Electrosurgical, Cutting & Coagulation & Accessories, Coagulator, Culdoscopic (and Accessories), Cannula And Trocar, Suprapubic, Non-disposable . Use the specialty filter in the sidebar to narrow results.