Solohealth, Inc. is one of 13048 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solohealth, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SOLOHEALTH STATION
1
Total
1
Cleared
0
Denied
Solohealth, Inc. has 1 FDA 510(k) cleared medical devices. Based in Duluth, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Solohealth, 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 - Solohealth, Inc.
1 devices