Continental Medical Laboratories, Inc.

Continental Medical Laboratories, Inc. — FDA 510(k) Submissions

Continental Medical Laboratories, Inc. has submitted 8 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 Staple, Removable (skin), General Surgery Tray, Suture Removal Kit, Wound Dressing Kit, Latex Patient Examination Glove . Use the specialty filter in the sidebar to narrow results.