Clearance Summary
ARACHNOPHLEBECTOMY NEEDLE received FDA 510(k) clearance under submission number K000932, sponsored by Advanced Medical Products, 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 2000-05-17.
- Submission: K000932
- Applicant / Sponsor: Advanced Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 2000-05-17
Classification & Regulation
This clearance is catalogued under FDA product code GAH and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.