Summa Therapeutics, LLC is one of 16294 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Summa Therapeutics, LLC - FDA 510(k) Cleared Devices
Recent clearances: Finesse™ Injectable PTA Balloon Dilatation Catheter, ComboCath OTW PTA Dilatation Catheter
2
Total
2
Cleared
0
Denied
Summa Therapeutics, LLC has 2 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Last cleared in 2023. Active since 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Summa Therapeutics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Caraballo Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Summa Therapeutics, LLC
2 devices