Clearance Summary
JOYKEY SURGICAL DRAPES (STERILE) received FDA 510(k) clearance under submission number K062480, sponsored by Joykey Industryial , Ltd.. 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 2007-03-05.
- Submission: K062480
- Applicant / Sponsor: Joykey Industryial , Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4370
- Decision date: 2007-03-05
Classification & Regulation
This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.