Micro-Aire Surgical Instruments, Inc.
Micro-Aire Surgical Instruments, Inc. — FDA 510(k) Submissions
Micro-Aire Surgical Instruments, Inc. has submitted 40 FDA 510(k) premarket notifications since 1981, of which 40 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/attachment, Blade, Saw, General & Plastic Surgery, Surgical, Bur, Surgical, General & Plastic Surgery, Motor, Surgical Instrument, Ac-powered, Handpiece, Air-powered, Dental . Use the specialty filter in the sidebar to narrow results.