Clearance Summary
PRE-POWDERED VINYL PATIENT EXAMINATION GLOVE, NON-STERILE received FDA 510(k) clearance under submission number K100977, sponsored by Jiangsu Sunshine Plastic Products, 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 2010-08-12.
- Submission: K100977
- Applicant / Sponsor: Jiangsu Sunshine Plastic Products, Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2010-08-12
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.