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

    SPECIFIC ATLAS MICROJUST

    K Number: K833324 · Decision Nov 14, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    48

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    Basic Information

    Device Name
    SPECIFIC ATLAS MICROJUST
    K Number
    K833324
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Haygood Scientific Tool Co.
    Date Received
    September 27, 1983
    Decision Date
    November 14, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N