Cleared Traditional

K180349 - AssureTech Panel Dip Tests, AssureTech Quick Cup Tests (FDA 510(k) Clearance)

Apr 2018
Decision
56d
Days
Class 2
Risk

K180349 is an FDA 510(k) clearance for the AssureTech Panel Dip Tests, 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. (Hangzhou) Co, Ltd. (Hangzhou, CN). The FDA issued a Cleared decision on April 5, 2018, 56 days after receiving the submission on February 8, 2018.

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

Submission Details

510(k) Number K180349 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 08, 2018
Decision Date April 05, 2018
Days to Decision 56 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

Similar Devices — NFT Test, Amphetamine, Over The Counter

All 27
Webest Multi-Drug Urine Cup
K260355 · WEBEST Biotech,, LLC · Mar 2026
SAFElife T-Cup Multi-Drug Urine Test Cup
K252550 · Guangzhou Wondfo Biotech Co., Ltd. · Nov 2025
VINScreen Urine Drug Test Cup
K252867 · Advin Biotech, Inc. · Oct 2025
Wisdiag Multi-Drug Urine Test Cup
K252554 · Vivachek Biotech (Hangzhou) Co., Ltd. · Sep 2025
CLUNGENE Multi-Drug Test Easy Cup
K252118 · Hangzhou Clongene Biotech Co., Ltd. · Aug 2025
AssureTech Quick Cup Tests
K252259 · Assure Tech., LLC · Aug 2025