Medical Device Manufacturer · US , Los Angeles , CA

Neurosigma, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2019

Total

Cleared

Denied

Neurosigma, Inc. has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Latest FDA clearance: Jan 2024. Active since 2019. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Neurosigma, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Neurosigma, Inc.

2 devices

1-2 of 2