Clearance Summary
VALLEYLAB MICROWAVE ABLATION GENERATOR received FDA 510(k) clearance under submission number K072687, sponsored by Covidien Lp, Formerly Know AS Valleylab, A Divison. 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 2008-11-25.
- Submission: K072687
- Applicant / Sponsor: Covidien Lp, Formerly Know AS Valleylab, A Divison
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2008-11-25
Classification & Regulation
This clearance is catalogued under FDA product code NEY and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.