CapsoVision, Inc.

CapsoVision, Inc. — FDA 510(k) Submissions

CapsoVision, Inc. has submitted 6 FDA 510(k) premarket notifications since 2016, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Imaging, Gastrointestinal, Wireless, Capsule . Use the specialty filter in the sidebar to narrow results.