Cryodyne Technologies, Inc.

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

Cryodyne Technologies, Inc. has submitted 6 FDA 510(k) premarket notifications since 1986, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Apparatus, Cell-freezing And Reagents, Apparatus, Roller, Stages, Microscope, Unit, Cryosurgical, Accessories, Gas, Calibration (specified Concentration) . Use the specialty filter in the sidebar to narrow results.