Clearance Summary
BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES received FDA 510(k) clearance under submission number K022091, sponsored by Tangshan Zhonghong Pulin Group 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 2002-12-30.
- Submission: K022091
- Applicant / Sponsor: Tangshan Zhonghong Pulin Group Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2002-12-30
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.