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

    TRANSPORT CULTURE MEDIUM DEVICE

    K Number: K120846 · Decision Jun 8, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    45
    Registration Numbers
    45
    Same Product Code
    62
    Applicant Total
    7
    Review Days
    80

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    Basic Information

    Device Name
    TRANSPORT CULTURE MEDIUM DEVICE
    K Number
    K120846
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2900
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Puritan Medical Products, LLC
    Date Received
    March 20, 2012
    Decision Date
    June 8, 2012
    Product Code
    LIO
    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
    LIO Device, Specimen Collection

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