Clearance Summary
ULTRACINCH ABLATION DEVICE, ULTRACINCH ACCESSORY PACK, MODELS UC-8, UC-9, UC-10, UC-11, UC-12, UC-13, UC-14, UC-ACC-1 received FDA 510(k) clearance under submission number K040641, sponsored by Epicor Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2004-05-05.
- Submission: K040641
- Applicant / Sponsor: Epicor Medical, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2004-05-05
Classification & Regulation
This clearance is catalogued under FDA product code NTB and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.