Clearance Summary
LATEX EXAMINATION GLOVE (POWDERED) received FDA 510(k) clearance under submission number K014280, sponsored by Brightway Gloves Pvt. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2002-03-20.
- Submission: K014280
- Applicant / Sponsor: Brightway Gloves Pvt. , Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2002-03-20
Classification & Regulation
This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.