Clearance Summary
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance under submission number K083047, sponsored by Zibo Wanci Plastic & Rubber Co., 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 2009-02-12.
- Submission: K083047
- Applicant / Sponsor: Zibo Wanci Plastic & Rubber Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2009-02-12
Classification & Regulation
This clearance is catalogued under FDA product code LYZ and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.