Aspen Labs

Aspen Labs — FDA 510(k) Submissions

Aspen Labs has submitted 6 FDA 510(k) premarket notifications since 1991, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Electrocautery, Gynecologic (and Accessories), Coagulator, Laparoscopic, Unipolar (and Accessories), Electrosurgical Device . Use the specialty filter in the sidebar to narrow results.