Clearance Summary
JIAWANG received FDA 510(k) clearance under submission number K140239, sponsored by Jiawang Glove 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 2014-06-12.
- Submission: K140239
- Applicant / Sponsor: Jiawang Glove Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 2014-06-12
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.