Intramed Laboratories, Inc.

Intramed Laboratories, Inc. — FDA 510(k) Submissions

Intramed Laboratories, Inc. has submitted 14 FDA 510(k) premarket notifications since 1987, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Valvulotome, Angioscope, Laparoscope, Gynecologic (and Accessories), Arthroscope, Dislodger, Stone, Basket, Ureteral, Metal . Use the specialty filter in the sidebar to narrow results.