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

    SCREENERS BARBITURATE TEST, DRUGSCREEN DIP BARBITURATE TEST

    K Number: K000522 · Decision Apr 18, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    88
    Registration Numbers
    88
    Same Product Code
    99
    Applicant Total
    8
    Review Days
    62

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    Basic Information

    Device Name
    SCREENERS BARBITURATE TEST, DRUGSCREEN DIP BARBITURATE TEST
    K Number
    K000522
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3150
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Drug Detection Devices, Ltd.
    Date Received
    February 16, 2000
    Decision Date
    April 18, 2000
    Product Code
    DIS
    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
    DIS Enzyme Immunoassay, Barbiturate

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    Other Clearances by Drug Detection Devices, Ltd.

    K Number Device Name
    K000452 SCREENERS METHAMPHETAMINE TEST, DRUGSCREEN DIP METHAMPHETAMINE TEST
    K000402 SCREENERS PHENCYCLIDINE (PCP) TEST, DRUGSCREEN DIP PHENCYCLIDINE (PCP) TEST
    K000400 SCREENERS AMPHETAMINE TEST, DRUGSCREEN DIP AMPHETAMINE TEST
    K000350 SCREENERS COCAINE TEST; DRUGSCREEN DIP COCAINE TEST
    K000273 SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST
    K000449 SCREENERS BENZODIAZEPINE (BZD) TEST, DRUG SCREEN DIP BENZODIAZEPINE (BZD) TEST
    K992949 SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST