Scientia Vascular, Inc.

Scientia Vascular, Inc. — FDA 510(k) Submissions

Scientia Vascular, Inc. has submitted 6 FDA 510(k) premarket notifications since 2023, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Guide, Wire, Catheter, Neurovasculature, Catheter, Percutaneous, Neurovasculature, Catheter, Thrombus Retriever . Use the specialty filter in the sidebar to narrow results.