Molded Products, Inc.

Molded Products, Inc. — FDA 510(k) Submissions

Molded Products, Inc. has submitted 7 FDA 510(k) premarket notifications since 1993, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tubing, Dialysate, Set, Administration, Intravascular, Accessories, Blood Circuit, Hemodialysis, Dialyzer, Capillary, Hollow Fiber, Protector, Transducer, Dialysis . Use the specialty filter in the sidebar to narrow results.