Clearance Summary
EPICOR ABLATION SYSTEM received FDA 510(k) clearance under submission number K080292, sponsored by St Jude Medical. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2008-07-25.
- Submission: K080292
- Applicant / Sponsor: St Jude Medical
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2008-07-25
Classification & Regulation
This clearance is catalogued under FDA product code OCL and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.