510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K260355Substantially Equivalent

Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup

WEBEST Biotech,, LLC, Irwindale CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K260355 is the FDA 510(k) clearance record for Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup, a class II device, cleared for WEBEST Biotech,, LLC on under FDA product code NFT (Test, Amphetamine, Over The Counter). FDA records list one 510(k) clearance for WEBEST Biotech,, LLC. As of , FDA records show no recalls naming K260355.

Clearance record

Decision date
Received
(34 days to decision)
Product code
NFT Test, Amphetamine, Over The Counter
Regulation
21 CFR 862.3100
Device class
Class II
Review panel
Clinical Toxicology
Applicant
WEBEST Biotech,, LLC 5350 Irwindale Ave., Irwindale CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NFT

Trailing 12 months
6 clearances under product code NFT in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NFT, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20261
August 20260
September 20261
October 20260