Soberlink Healthcare, LLC is one of 13271 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Soberlink Healthcare, LLC - FDA 510(k) Cleared Devices
Recent clearances: Soberlink Cellular Device and Sober Sky Web Portal
1
Total
1
Cleared
0
Denied
Soberlink Healthcare, LLC has 1 FDA 510(k) cleared medical devices. Based in Huntington Beach, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Soberlink Healthcare, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Obelix Consulting, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Soberlink Healthcare, LLC
1 devices