Piper Access, LLC

Piper Access, LLC — FDA 510(k) Submissions

Piper Access, LLC has submitted 3 FDA 510(k) premarket notifications since 2018, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Hypodermic, Single Lumen, Midline Catheter, Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days . Use the specialty filter in the sidebar to narrow results.