VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup— 510(k) K252867

Name: FDA 510(k) clearance K252867
Creator: U.S. Food and Drug Administration
Published: 2025-10-09

Substantially Equivalent

Advin Biotech, Inc.

FDA 510(k) clearance K252867 for VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup, Substantially Equivalent on 2025-10-09. Applicant: Advin Biotech, Inc.. Device class: 2.

Clearance details

Applicant: Advin Biotech, Inc.
Product code: Code NFT
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 2025-09-09
Decision date: 2025-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, 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.