Neurosigma, Inc. - FDA 510(k) Cleared Devices
2
Total
1
Cleared
1
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.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Neurosigma, Inc.
2 devices