Harvest Technologies, Corp.

Harvest Technologies, Corp. — FDA 510(k) Submissions

Harvest Technologies, Corp. has submitted 6 FDA 510(k) premarket notifications since 2001, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Syringe, Piston, Centrifuges (micro, Ultra, Refrigerated) For Clinical Use, Bone Grafting Material, Synthetic, System, Suction, Lipoplasty . Use the specialty filter in the sidebar to narrow results.