Sanguina, LLC is one of 13048 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sanguina, LLC - FDA 510(k) Cleared Devices
Recent clearances: AnemoCheck
1
Total
1
Cleared
0
Denied
Sanguina, LLC has 1 FDA 510(k) cleared medical devices. Based in Atlanta, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Sanguina, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cambria Regulatory Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sanguina, LLC
1 devices