Microbio-Medics, Inc.

Microbio-Medics, Inc. — FDA 510(k) Submissions

Microbio-Medics, Inc. has submitted 13 FDA 510(k) premarket notifications since 1988, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Replacement, Ossicular Prosthesis, Total, Drape, Surgical, Splint, Nasal, Prosthesis, Partial Ossicular Replacement, Tubes, Vials, Systems, Serum Separators, Blood Collection . Use the specialty filter in the sidebar to narrow results.