FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

Evidence MultiSTAT DOA Urine MultiPlex

K Number: K250741 · Decision Jan 23, 2026
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
214
Applicant Total
18
Review Days
318

Basic Information

Device Name
Evidence MultiSTAT DOA Urine MultiPlex
K Number
K250741
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3650
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Randox Laboratories Limited
Date Received
March 11, 2025
Decision Date
January 23, 2026
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

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K Number Device Name
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K140971 LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS LEVEL 1,2 AND LEVEL 3.
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K140522 RANDOX IMMUNOASSAY PREMIUM PLUS CONTROL LEVELS 1,2 AND LEVEL 3 AND IMMUNOASSAY PREMIUM PLUS TRI-LEVEL CONTROL
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