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510(k) Data Aggregation

    K Number
    K960539
    Device Name
    DIAO HAND SURGERY SET
    Date Cleared
    1996-07-23

    (167 days)

    Product Code
    Regulation Number
    888.4540
    Why did this record match?
    Product Code :

    HXB

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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