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510(k) Data Aggregation

    K Number
    K960669
    Manufacturer
    Date Cleared
    1996-07-12

    (143 days)

    Product Code
    Regulation Number
    866.5510
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    HYDRAGEL IF, 6 IF, 12 IF PENTA KITS/HYDRAGEL IF, DOUBLE IF, 2 IF, & 4 IF KITS

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