Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup— 510(k) K260355

Name: FDA 510(k) clearance K260355
Creator: U.S. Food and Drug Administration
Published: 2026-03-09

Substantially Equivalent

WEBEST 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.

Clearance details

Applicant: WEBEST Biotech,, LLC
Product code: Code NFT
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 2026-02-03
Decision date: 2026-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irwindale, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.