K260355
- 510(k) number
- K260355
- Device name
- Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup
- Applicant
- WEBEST Biotech,, LLC CA · US
- Product code
- NFT — Test, Amphetamine, Over The Counter
- Decision date
- 2026-03-09
- Date received
- 2026-02-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Toxicology
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K260355.pdf
Official FDA record: K260355
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.