Sleep Modus, Inc. is one of 22702 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sleep Modus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ActiSpec Activity Monitor
1
Total
1
Cleared
0
Denied
Sleep Modus, Inc. has 1 FDA 510(k) cleared medical devices. Based in Richardson, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Sleep Modus, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ken Block Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Sleep Modus, Inc.
1 devices