Clearance Summary
Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro received FDA 510(k) clearance under submission number K250067, sponsored by Guangzhou Decheng Biotechnology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Toxicology review panel. The statutory decision date of record is 2025-02-20.
- Submission: K250067
- Applicant / Sponsor: Guangzhou Decheng Biotechnology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Toxicology
- Device class: Class II
- Regulation citation: 21 CFR 862.3650
- Decision date: 2025-02-20
Classification & Regulation
This clearance is catalogued under FDA product code NGL and 21 CFR 862.3650, within the Clinical Toxicology review panel as a Class II device.