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

    APTUS BLUE

    K Number: K030884 · Decision May 27, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35
    Same Product Code
    40
    Applicant Total
    1
    Review Days
    68

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    Basic Information

    Device Name
    APTUS BLUE
    K Number
    K030884
    Device Class
    FDA unclassified
    Clearance Type
    Abbreviated
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Acadental
    Date Received
    March 20, 2003
    Decision Date
    May 27, 2003
    Product Code
    KJJ
    Advisory Committee
    Unknown
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KJJ Cleanser, Root Canal

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