Mill-Rose Laboratory

Mill-Rose Laboratory — FDA 510(k) Submissions

Mill-Rose Laboratory has submitted 46 FDA 510(k) premarket notifications since 1979, of which 44 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Bronchoscope (flexible Or Rigid), Forceps, General & Plastic Surgery, Electrosurgical, Cutting & Coagulation & Accessories, Endoscopic Injection Needle, Gastroenterology-urology, Snare, Flexible . Use the specialty filter in the sidebar to narrow results.