Neurospectrum, LLC is one of 19694 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurospectrum, LLC - FDA 510(k) Cleared Devices
Recent clearances: Neurosplint
1
Total
1
Cleared
0
Denied
Neurospectrum, LLC has 1 FDA 510(k) cleared medical devices. Based in Rancho Mirage, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Neurospectrum, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nu Device Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Neurospectrum, LLC
1 devices