Wavestate, Inc. is one of 24654 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wavestate, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WAVESTATE NEUROMONITOR
1
Total
1
Cleared
0
Denied
Wavestate, Inc. has 1 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Wavestate, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Wavestate, Inc.
1 devices