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510(k) Data Aggregation

    K Number
    K161188
    Device Name
    HEPATIQ 1.1
    Manufacturer
    Date Cleared
    2016-06-09

    (43 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    HEPATIQ is a nuclear medicine software application used to display and process liver-spleen images. The results obtained may be used as a tool, by a nuclear physician, in quantifying liver-spleen images. The data processed may be derived from any nuclear medicine liver-spleen procedure. The HEPATIQ software should only be used by qualified nuclear medicine professionals.

    Device Description

    HEPATIQ is a nuclear medicine software application used to display and process liver-spleen images.

    AI/ML Overview

    I am sorry, but the provided text from the FDA 510(k) summary for HEPATIQ 1.1 does not contain the detailed information required to describe the acceptance criteria and the study that proves the device meets those criteria.

    The document is a letter from the FDA to HEPATIQ LLC confirming the substantial equivalence of their device to a predicate device, and includes the "Indications for Use" for HEPATIQ 1.1.

    It does not include:

    1. A table of acceptance criteria and reported device performance.
    2. Sample sizes for test or training sets, nor data provenance.
    3. Information on experts used for ground truth (number or qualifications).
    4. Adjudication methods.
    5. Findings from an MRMC comparative effectiveness study or effect sizes.
    6. Details of a standalone algorithm performance study.
    7. The type of ground truth used (e.g., pathology, outcomes data).
    8. How ground truth for the training set was established.

    Therefore, I cannot fulfill your request for this specific information based on the provided text.

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