Clearance Summary
EARLOOP FACE MASK received FDA 510(k) clearance under submission number K990719, sponsored by Shuenn Bao Shing Corp.. 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 1999-07-12.
- Submission: K990719
- Applicant / Sponsor: Shuenn Bao Shing Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4040
- Decision date: 1999-07-12
Classification & Regulation
This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.