Neuroqore, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuroqore, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NQ TMS for MDD (NQv1-MU-01)
1
Total
1
Cleared
0
Denied
Neuroqore, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Last cleared in 2023. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuroqore, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Makromed, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Neuroqore, Inc.
1 devices