FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ARK Hydrocodone Assay

K Number: K231752 · Decision Nov 9, 2023
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
214
Applicant Total
17
Review Days
147

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Basic Information

Device Name
ARK Hydrocodone Assay
K Number
K231752
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3650
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ark Diagnostics, Inc.
Date Received
June 15, 2023
Decision Date
November 9, 2023
Product Code
DJG
Advisory Committee
Clinical Toxicology
Review Advisory Committee
CH
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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K182280 ARK Tramadol Assay
K182779 ARK EDDP Assay
K180427 ARK Fentanyl Assay
K163359 ARK Methotrexate Assay
DEN160033 ARK Voriconazole II Assay Test System
K153596 ARK Oxcarbazepine Metabolite Assay, ARK Oxcarbazepine Metabolite Calibrator, ARK Oxcarbazepine Metabolite Control
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