K250067
- 510(k) number
- K250067
- Device name
- Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup Pro
- Applicant
- Guangzhou Decheng Biotechnology Co., Ltd. CN
- Product code
- NGL — Test, Opiates, Over The Counter
- Decision date
- 2025-02-20
- Date received
- 2025-01-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Toxicology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K250067.pdf
Official FDA record: K250067
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.