Niveus Medical, Inc. is one of 19020 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Niveus Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Muscle Stimulation System 110, MUSCLE STIMULATION SYSTEM
2
Total
2
Cleared
0
Denied
Niveus Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Hillsboroguh, US.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Niveus Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Domecus Consulting Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Niveus Medical, Inc.
2 devices