Neuromed Devices, Inc. is one of 21528 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuromed Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NEUROCALM MODEL 1 AND 2
1
Total
1
Cleared
0
Denied
Neuromed Devices, Inc. has 1 FDA 510(k) cleared medical devices. Based in Laguna Niguel, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuromed Devices, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Neuromed Devices, Inc.
1 devices