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

LYHER® Urine Multi-Drug Test Kit(Cup), LYHER® Urine Multi-Drug Test Kit(Cassette), LYHER® Urine Multi-Drug Test Kit(Dipcard)

K Number: K232597 · Decision Jan 9, 2024
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
214
Applicant Total
3
Review Days
134

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Basic Information

Device Name
LYHER® Urine Multi-Drug Test Kit(Cup), LYHER® Urine Multi-Drug Test Kit(Cassette), LYHER® Urine Multi-Drug Test Kit(Dipcard)
K Number
K232597
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3650
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hangzhou Laihe Biotech Co., Ltd.
Date Received
August 28, 2023
Decision Date
January 9, 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

Other 510(k) clearances with the same product code (DJG), ordered by most recent decision date.

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Other Clearances by Hangzhou Laihe Biotech Co., Ltd.

K Number Device Name
K240287 LYHER® Oral fluid Multi-Drug Test Kit (Cube)
K232604 LYHER® Urine Marijuana (THC) Test Kit (Strip), LYHER® Urine Marijuana (THC) Test Kit (Cassette)