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

BioSieve™ Fentanyl FIA Test Kit; BioSieve™ ToxiSmart FIA Reader

K Number: K240124 · Decision Jun 14, 2024
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
214
Applicant Total
10
Review Days
150

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Basic Information

Device Name
BioSieve™ Fentanyl FIA Test Kit; BioSieve™ ToxiSmart FIA Reader
K Number
K240124
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3650
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vivachek Biotech (Hangzhou) Co., Ltd.
Date Received
January 16, 2024
Decision Date
June 14, 2024
Product Code
DJG
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
DJG Enzyme Immunoassay, Opiates

Similar 510(k) Clearances

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Other Clearances by Vivachek Biotech (Hangzhou) Co., Ltd.

K Number Device Name
K261280 BioSieve Multi-Drug Urine Test Panel;BioSieve Multi-Drug Urine Home Test Panel
K252554 Wisdiag Multi-Drug Urine Test Cup; Wisdiag Multi-Drug Urine Home Test Cup
K241869 BioSieve™ Fentanyl FIA Home Test Kit; BioSieve™ Fentanyl FIA Pro Test Kit; BioSieve™ Toxismart Reader
K222126 VivaChek™ Fad Blood Glucose Monitoring System, VivaChek™ Fad Smart Blood Glucose Monitoring System, VivaChek™ Fad Sync Blood Glucose Monitoring System
K233058 VivaChek Link Plus Blood Glucose Monitoring System
K233062 BioSieveTM Multi-Drug Urine Test Panel; BioSieveTM Multi-Drug Urine Test Panel Rx
K231978 BioSieve™ Marijuana Test Panel 50; BioSieve™ Marijuana Test Strip 50; BioSieve™ Dx Marijuana Test Strip 20; BioSieve™ Dx Marijuana Test Strip 50; BioSieve™ Dx Marijuana Test Panel 20; BioSieve™ Dx Marijuana Test Panel 50
K222667 Wisdiag Multi-Drug Urine Test Cup, Wisdiag Multi-Drug Urine Test Cup Rx
K192957 VivaChek Blood Glucose and B-Ketone Monitoring System