Clearance Summary
SURGICAL BLADES received FDA 510(k) clearance under submission number K880244, sponsored by Ailee C/O Havel'S, 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 1988-02-10.
- Submission: K880244
- Applicant / Sponsor: Ailee C/O Havel'S, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1988-02-10
Classification & Regulation
This clearance is catalogued under FDA product code GES and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.