Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup— 510(k) K260355
Substantially EquivalentWEBEST Biotech,, LLC
FDA 510(k) clearance K260355 for Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup, Substantially Equivalent on 2026-03-09. Applicant: WEBEST Biotech,, LLC. Device class: 2.
Summary
WEBEST Biotech's record covers the Webest Multi-Drug Urine Cup and the Webest Home Multi-Drug Urine Cup, filed under NFT, over-the-counter amphetamine tests. The record doesn't list which drugs the cups test for.
Class II, 21 CFR 862.3100. Clinical Toxicology is both the classification panel and the review panel. It was a Traditional 510(k).
WEBEST Biotech filed from Irwindale, California. The decision came 34 calendar days after receipt (February 3 to March 9, 2026).
Clearance details
- Applicant
- WEBEST Biotech,, LLC
- Product code
- Product code NFT
- Device class
- Class 2
- Regulation
- 21 CFR 862.3100
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irwindale, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.