BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    GRAM NEGATIVE FLUORESCENT IDENTIFICATION PANEL

    K Number: K862642 · Decision Sep 11, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    6
    Applicant Total
    24
    Review Days
    62

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    Basic Information

    Device Name
    GRAM NEGATIVE FLUORESCENT IDENTIFICATION PANEL
    K Number
    K862642
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2660
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    American Micro Scan
    Date Received
    July 11, 1986
    Decision Date
    September 11, 1986
    Product Code
    LQM
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LQM Gram Negative Identification Panel

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