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

    URINE CANNABINOIDS SCREEN FLEX(TM) REAGENT CARTRIDGE

    K Number: K950181 · Decision Apr 5, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    103
    Registration Numbers
    103
    Same Product Code
    149
    Applicant Total
    253
    Review Days
    78

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    Basic Information

    Device Name
    URINE CANNABINOIDS SCREEN FLEX(TM) REAGENT CARTRIDGE
    K Number
    K950181
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3870
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    E.I. Dupont DE Nemours & Co., Inc.
    Date Received
    January 17, 1995
    Decision Date
    April 5, 1995
    Product Code
    LDJ
    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
    LDJ Enzyme Immunoassay, Cannabinoids

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    Other Clearances by E.I. Dupont DE Nemours & Co., Inc.

    K Number Device Name
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    K951441 DUPONT ACA DIGOXIN (DGN A) METHOD
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