Clearance Summary
VES 1501-M received FDA 510(k) clearance under submission number K982409, sponsored by Angiolaz, 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 1998-08-21.
- Submission: K982409
- Applicant / Sponsor: Angiolaz, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4160
- Decision date: 1998-08-21
Classification & Regulation
This clearance is catalogued under FDA product code FWF and 21 CFR 878.4160, within the General, Plastic Surgery review panel as a Class I device.