Gaymar Industries, Inc.

Gaymar Industries, Inc. — FDA 510(k) Submissions

Gaymar Industries, Inc. has submitted 27 FDA 510(k) premarket notifications since 1976, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Thermal Regulating, Pack, Hot Or Cold, Water Circulating, Mattress, Air Flotation, Alternating Pressure, Sleeve, Limb, Compressible, Bed, Air Fluidized . Use the specialty filter in the sidebar to narrow results.