Clearance Summary
BRIGHTWAY BRAND LATEX SURGICAL GLOVES - STERILE (POWDER FREE) received FDA 510(k) clearance under submission number K992021, sponsored by Brightsway Holdings Sdn Bhd. 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 1999-07-23.
- Submission: K992021
- Applicant / Sponsor: Brightsway Holdings Sdn Bhd
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4460
- Decision date: 1999-07-23
Classification & Regulation
This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.