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510(k) Data Aggregation

    K Number
    K042887
    Device Name
    ACCU-CHEK SPIRIT
    Date Cleared
    2005-03-18

    (150 days)

    Product Code
    Regulation Number
    880.5725
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ACCU-CHEK SPIRIT

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

    The ACCU-CHEK Spirit Insulin Infusion Pump is intended for the subcutaneous continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin as prescribed by a physician.

    Device Description

    The ACCU-CHEK Spirit Insulin Infusion Pump is an external, portable insulin pump designed for continuous delivery of insulin. The design allows the delivery of 0.1 to 25.0 units of U100 insulin per hour in basal rates and up to 25.00 units of U100 insulin per meal or meal bolus.

    AI/ML Overview

    The provided text does not contain specific acceptance criteria, study details, or performance metrics for the ACCU-CHEK Spirit Insulin Infusion Pump.

    The document is a 510(k) summary and FDA clearance letter, which primarily focuses on establishing substantial equivalence to predicate devices rather than presenting detailed performance studies with acceptance criteria.

    The only statement related to device performance is a general claims that "Testing of the ACCU-CHEK Spirit demonstrated that the device meets the resuirements for its intended use. The data also demonstrates that the ACCU-CHEK Spirit is substantially equivalent to the predicate devices." No specific criteria or reported performance values are given.

    Therefore, I cannot provide the requested table and detailed information about the study as the necessary data is not present in the provided text.

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