Clearance Summary
POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE received FDA 510(k) clearance under submission number K082598, 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 2009-01-07.
- Submission: K082598
- 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: 2009-01-07
Classification & Regulation
This clearance is catalogued under FDA product code LZA and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.