Dlp, Inc.

Dlp, Inc. — FDA 510(k) Submissions

Dlp, Inc. has submitted 56 FDA 510(k) premarket notifications since 1979, of which 56 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass, Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass, Needle, Aspiration And Injection, Disposable, Instrument, Biopsy, Instruments, Surgical, Cardiovascular . Use the specialty filter in the sidebar to narrow results.