Clearance Summary
Powder Free Nitrile Examination Gloves, Orange received FDA 510(k) clearance under submission number K220229, sponsored by Shanxi Hongjin Plastic Technology 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 2022-03-26.
- Submission: K220229
- Applicant / Sponsor: Shanxi Hongjin Plastic Technology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2022-03-26
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.