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510(k) Data Aggregation

    K Number
    K022911
    Device Name
    MODEL AMI1200 C-ARM
    Manufacturer
    INTEGRITY PRACTICE MANAGEMENT, INC.
    Date Cleared
    2002-12-02

    (90 days)

    Product Code
    JAA
    Regulation Number
    892.1650
    Why did this record match?
    Applicant Name (Manufacturer) :

    INTEGRITY PRACTICE MANAGEMENT, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The AMI1200 is intended to be used only by licensed practitioners; to produce imaging techniques required, providing the patient with an adequate diagnosis of their presented condition.
    Device Description
    Not Found
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