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

ARK EDDP Assay

K Number: K182779 · Decision Nov 21, 2018
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
62
Applicant Total
17
Review Days
51

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Basic Information

Device Name
ARK EDDP Assay
K Number
K182779
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3620
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ark Diagnostics, Inc.
Date Received
October 1, 2018
Decision Date
November 21, 2018
Product Code
DJR
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
DJR Enzyme Immunoassay, Methadone

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K200197 ARK Fentanyl II Assay
K182280 ARK Tramadol 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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