C2 Therapeutics, Inc.
C2 Therapeutics, Inc. holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2018, with 1 FDA device recall on record.
Top product codes for C2 Therapeutics, Inc.
FDA recalls by C2 Therapeutics, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by C2 Therapeutics, Inc.
- K163684 — C2 CryoBalloon Ablation System
- K161202 — C2 Cryoballoon Ablation System
- K160994 — C2 CryoBalloon Focal Pear Catheter
- K152329 — Coldplay Cryoballoon; Focal Ablation System, Full Ablation System; Swipe Ablation System
- K153541 — Coldplay CryoBalloon® Ablation System
- K152140 — Boa Endoscopic Valve
- K151054 — Coldplay Full CryoBalloon Ablation System and Coldplay Swipe CryoBalloon Ablation System
Data sourced from openFDA. This site is unofficial and independent of the FDA.