Summa Therapeutics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Summa Therapeutics - FDA 510(k) Cleared Devices
Recent clearances: Finesse Injectable™ PTA Balloon Dilatation Catheter
1
Total
1
Cleared
0
Denied
Summa Therapeutics has 1 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Latest FDA clearance: Jul 2024. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Summa Therapeutics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Summa Therapeutics
1 devices