Arbor Technologies, Inc.

Arbor Technologies, Inc. — FDA 510(k) Submissions

Arbor Technologies, Inc. has submitted 10 FDA 510(k) premarket notifications since 1986, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Filter, Conduction, Anesthetic, Filter, Infusion Line, Apparatus, Suction, Operating-room, Wall Vacuum Powered, Evacuator, Vapor, Cement Monomer, Insufflator, Laparoscopic . Use the specialty filter in the sidebar to narrow results.