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

FDA 510(k) K241741 · Guangzhou Wondfo Biotech Co., Ltd.

Substantially Equivalent

510(k) numberK241741

Submission

Device name
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
Applicant
Guangzhou Wondfo Biotech Co., Ltd.
Guangzhou, CN
Received
June 17, 2024
Decision date
July 16, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NGL – Test, Opiates, Over The Counter
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3650
Specialty
Clinical Toxicology

Other 510(k)s with product code NGL

510(k)DeviceApplicantDecision
K253567Healgen Accurate Urine Drug Screen Dip Card; Healgen Accurate Home Urine Drug Test Dip…NGL · Traditional Healgen Scientific,, LLC12/23/2025SE
K250803Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test CupNGL · Traditional Anhui Deepblue Medical Technological Co., Ltd.04/15/2025SE
K250067Dochek® Multi-Drug Urine Test Cup; Dochek® Multi-Drug Urine Test Cup ProNGL · Traditional Guangzhou Decheng Biotechnology Co., Ltd.02/20/2025SE
K242428Dochek® Fentanyl Urine Test Strip, Dochek® Fentanyl Urine Test Strip Plus, Dochek®…NGL · Traditional Guangzhou Decheng Biotechnology Co., Ltd.02/06/2025SE
K243365Healgen Accurate Muti-Drug Urine Drug Screen Cup; Healgen Accurate Home Muti-Drug Urine…NGL · Traditional Healgen Scientific,, LLC12/17/2024SE
K243064ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl…NGL · Traditional Eterbio, Inc.11/20/2024SE
K242802CLUNGENE Fentanyl Home Test Cassette; CLUNGENE Fentanyl Test CassetteNGL · Traditional Hangzhou Clongene Biotech Co., Ltd.11/08/2024SE
K241869BioSieve™ Fentanyl FIA Home Test Kit; BioSieve™ Fentanyl FIA Pro Test Kit; BioSieve™…NGL · Traditional Vivachek Biotech (Hangzhou) Co., Ltd.10/04/2024SE
K241969Hightop® Home Use Fentanyl/Norfentanyl Urine Rapid Test Panel; Hightop®…NGL · Traditional Qingdao Hightop Biotech Co., Ltd.08/14/2024SE
K241100Rapid Urine Fentanyl (FYL) Test Strip; Rapid Urine Fentanyl (FYL) Test DipcardNGL · Traditional Co-Innovation Biotech Co., Ltd.05/22/2024SE

More from Co-Innovation Biotech Co., Ltd.

510(k)DeviceDecision
K260065SAFElife T-Dip Multi-Drug Urine Test Panel; SAFElife T-Dip Multi-Drug Urine Test Panel DxNFT · Traditional 04/28/2026SE
K252550SAFElife T-Cup Multi-Drug Urine Test Cup; SAFElife T-Cup Multi-Drug Urine Test Cup DxNFT · Traditional 11/18/2025SE
K251289WELLlife COVID-19 Antigen Test RxQVF · Dual Track 10/22/2025SE
K241317Wondfo 2019-nCoV Antigen Test (Lateral Flow Method)QYT · Traditional 09/30/2024SE
K202567Wondfo T-Dip Multi-Drug Urine Test Panel, Wondfo T-Dip Multi-Drug Urine Test Panel RxNFT · Traditional 09/25/2020SE
K182701Wondfo T-Cup Multi-Drug Urine Test CupNFT · Traditional 12/03/2018SE
K173229Preview Digital Pregnancy TestLCX · Traditional 03/12/2018SE
K162333Wondfo One Step Fecal Occult Blood (FOB) TestKHE · Traditional 05/14/2017SE
K161214Wondfo Amphetamine Urine Test AMP 500 (Cup, Dipcard), Wondfo Cocaine Urine Test COC…DIO · Traditional 06/27/2016SE
K152495Wondfo Propoxyphene Urine TestJXN · Traditional 11/23/2015SE

Questions and answers

When was 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 cleared by the FDA?

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 (K241741) received a 510(k) decision of Substantially Equivalent on July 16, 2024, 29 days after the submission was received.

What is the product code of K241741?

The FDA product code is NGL – Test, Opiates, Over The Counter, a Class II (moderate risk) device regulated under 21 CFR 862.3650.