C2 Therapeutics is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
C2 Therapeutics - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
C2 Therapeutics has 3 FDA 510(k) cleared medical devices. Based in Redwood, Ca, US.
Historical record: 3 cleared submissions from 2010 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by C2 Therapeutics Filter by specialty or product code using the sidebar.
C2 Therapeutics — FDA 510(k) Products and Clearance History
3 devices
Cleared
Apr 14, 2015
Sidecar External Working Channel
Gastroenterology & Urology
89d
Cleared
Aug 22, 2013
CRYOBALLOON FOCAL ABLATION SYSTEM
General & Plastic Surgery
86d
Cleared
Sep 29, 2010
CRYOBALLOON ABLATION SYSTEM
General & Plastic Surgery
90d