Clearance Summary
AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007 received FDA 510(k) clearance under submission number K003978, sponsored by Afx, 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 2001-05-22.
- Submission: K003978
- Applicant / Sponsor: Afx, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2001-05-22
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.