Medical Device Manufacturer · US , Los Angeles , CA

Neurosigma, Inc.

2 submissions · 1 cleared · Since 2019
2
Total
1
Cleared
1
Denied

Neurosigma, Inc. — FDA 510(k) Submissions

Neurosigma, Inc. has submitted 2 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Transcutaneous Nerve Stimulator For Adhd . Use the specialty filter in the sidebar to narrow results.

2 devices
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