Pilling Co.

Pilling Co. — FDA 510(k) Submissions

Pilling Co. has submitted 39 FDA 510(k) premarket notifications since 1976, of which 39 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instruments, Surgical, Cardiovascular, Light Source, Fiberoptic, Routine, Catheter, Continuous Flush, Clamp, Vascular, Stripper, Artery, Intraluminal . Use the specialty filter in the sidebar to narrow results.