Cleared Traditional

K252259 - AssureTech Quick Cup Tests (FDA 510(k) Clearance)

Also includes:
AssureTech Multi-drug Urine Test Cup
Aug 2025
Decision
25d
Days
Class 2
Risk

K252259 is an FDA 510(k) clearance for the AssureTech Quick Cup Tests. This device is classified as a Test, Amphetamine, Over The Counter (Class II - Special Controls, product code NFT).

Submitted by Assure Tech., LLC (Wilmington, US). The FDA issued a Cleared decision on August 15, 2025, 25 days after receiving the submission on July 21, 2025.

This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3100.

Submission Details

510(k) Number K252259 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 21, 2025
Decision Date August 15, 2025
Days to Decision 25 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF

Device Classification

Product Code NFT - Test, Amphetamine, Over The Counter
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.3100