FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

SAFElife T-Dip Multi-Drug Urine Test Panel; SAFElife T-Dip Multi-Drug Urine Test Panel Dx

K Number: K260065 · Decision Apr 28, 2026
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
29
Applicant Total
43
Review Days
109

Basic Information

Device Name
SAFElife T-Dip Multi-Drug Urine Test Panel; SAFElife T-Dip Multi-Drug Urine Test Panel Dx
K Number
K260065
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guangzhou Wondfo Biotech Co., Ltd.
Date Received
January 9, 2026
Decision Date
April 28, 2026
Product Code
NFT
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NFT Test, Amphetamine, Over The Counter

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K Number Device Name
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K241741 SAFElife™ Fentanyl Urine Home Test (Cassette); SAFElife™ Fentanyl (FTY) Urine Test Cassette; SAFElife™ T-Dip Fentanyl Urine Home Test (Dip Card); SAFElife™ T-Dip Fentanyl (FTY) Urine Test Panel
K202567 Wondfo T-Dip Multi-Drug Urine Test Panel, Wondfo T-Dip Multi-Drug Urine Test Panel Rx
K182701 Wondfo T-Cup Multi-Drug Urine Test Cup
K173229 Preview Digital Pregnancy Test
K162333 Wondfo One Step Fecal Occult Blood (FOB) Test
K161214 Wondfo Amphetamine Urine Test AMP 500 (Cup, Dipcard), Wondfo Cocaine Urine Test COC 150(Cup, Dipcard), Wondfo Methamphetamine Urine Test MET 500 (Cup, Dipcard)
K152495 Wondfo Propoxyphene Urine Test
Search all 43 clearances from Guangzhou Wondfo Biotech Co., Ltd. →