Clearance Summary
PRE-POWDERED NON-STERILE VINYL EXAMINATION GLOVES received FDA 510(k) clearance under submission number K042213, sponsored by Shandong Perfect Plastic 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 2004-09-09.
- Submission: K042213
- Applicant / Sponsor: Shandong Perfect Plastic Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2004-09-09
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.