Clearance Summary
NON-STERILE POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE received FDA 510(k) clearance under submission number K042378, sponsored by Shijiazhuang Tillotson Rubber 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 2004-09-20.
- Submission: K042378
- Applicant / Sponsor: Shijiazhuang Tillotson Rubber Products Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2004-09-20
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.