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

    MEDTOX OXYCODONE

    K Number: K060351 · Decision May 12, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    100
    Registration Numbers
    100
    Same Product Code
    214
    Applicant Total
    22
    Review Days
    88

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    Basic Information

    Device Name
    MEDTOX OXYCODONE
    K Number
    K060351
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3650
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medtox Diagnostics, Inc.
    Date Received
    February 13, 2006
    Decision Date
    May 12, 2006
    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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    Other Clearances by Medtox Diagnostics, Inc.

    K Number Device Name
    K252684 Labcorp Fentanyl Urine Visual Test
    K100951 MEDTOX BUPRENORPHINE TEST
    K100023 PROFILE-V MEDTOXSCAN DRUGS OF ABUSE TEST SYSTEM AND 12 DRUGS TEST SYSTEM
    K091454 PROFILE-V MEDTOXSCAN DRUGS OF ABUSE TEST SYSTEM
    K080635 MEDTOXSCAN
    K050394 SURE-SCREEN AMPHETAMINE, BENZODIAZEPINE, COCAINE, METHAMPHETAMINE/MDMA, METHADONE, OPIATES, PHENCYCLIDINE & CANNABINOIDS
    K033334 PROFILE -ER
    K031032 VERDICT II, PROFILE II
    K022141 VERDICT-II
    K020787 VERDICT-II PROPOXYPHENE
    Search all 22 clearances from Medtox Diagnostics, Inc. →