Medical Device Manufacturer · US , Stamford , CT

Vivosonic, Inc.

5 submissions · 5 cleared · Since 2001
5
Total
5
Cleared
0
Denied

Vivosonic, Inc. — FDA 510(k) Submissions

Vivosonic, Inc. has submitted 5 FDA 510(k) premarket notifications since 2001, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Auditory, Evoked Response, Audiometer . Use the specialty filter in the sidebar to narrow results.

5 devices
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All5 Ear, Nose, Throat 3 Neurology 2