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510(k) Data Aggregation

    K Number
    K964423
    Device Name
    AXIOM INF
    Date Cleared
    1997-01-24

    (112 days)

    Product Code
    Regulation Number
    890.5850
    Why did this record match?
    Applicant Name (Manufacturer) :

    AXIOM MANUFACTURING

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K955146
    Device Name
    AXIOM-HVG
    Date Cleared
    1996-05-17

    (186 days)

    Product Code
    Regulation Number
    890.5850
    Why did this record match?
    Applicant Name (Manufacturer) :

    AXIOM MANUFACTURING

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

    Ask a specific question about this device

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