Stentor, Inc.

Stentor, Inc. — FDA 510(k) Submissions

Stentor, Inc. has submitted 3 FDA 510(k) premarket notifications since 1999, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Image Processing, Radiological, System, Digital Image Communications, Radiological . Use the specialty filter in the sidebar to narrow results.