Venospital, Inc.

Venospital, Inc. — FDA 510(k) Submissions

Venospital, Inc. has submitted 14 FDA 510(k) premarket notifications since 1977, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Set, Administration, Intravascular, Set, Transfer (blood/plasma), Needle, Fistula . Use the specialty filter in the sidebar to narrow results.