Documento fuente o registro público
FDA 510(k) K250067 — Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro
FDA 510(k) index record K250067. Device: Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro. Applicant as listed: Guangzhou Decheng Biotechnology Co., Ltd.. Decision date: 2025-02-20.
Fuente
"device_name": "Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro"
Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.
Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K250067.
Device name: Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro. Applicant as listed: Guangzhou Decheng Biotechnology Co., Ltd..
Decision date: 2025-02-20. Decision wording: Substantially Equivalent.
Product code: NGL. Regulation: 21 CFR 862.3650. Medical specialty: Clinical Toxicology.
This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.
Interested in these solutions?
Submit a sourcing request with the assays, volumes, and timeline of your own project.