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510(k) Data Aggregation

    K Number
    K100031
    Date Cleared
    2010-07-19

    (194 days)

    Product Code
    Regulation Number
    864.6550
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    IND ONE STEP FECAL OCCULT BLOOD TEST MODEL 440-10

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

    The One Step Fecal Occult Blood (FOB) Test is a simple, direct binding immunoassay for the rapid and the qualitative detection of fecal occult blood by laboratories or physician's offices. It is useful to determine gastrointestinal bleeding found in gastrointestinal disorders. For professional in vitro diagnostic use only.

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for the "IND One Step Fecal Occult Blood Test." It primarily states that the device has been found substantially equivalent to a legally marketed predicate device.

    Unfortunately, this document does not contain the detailed information necessary to answer your specific questions regarding acceptance criteria, study design, reported device performance, sample sizes, ground truth establishment, or multi-reader multi-case studies.

    This type of information is typically found in the 510(k) submission itself, or in supplementary documents such as clinical study reports or performance verification reports, which are not included in this letter.

    Therefore, I cannot provide the requested table and details based solely on the provided text. The document confirms the device's clearance but does not elaborate on the specific performance data or study methodology used to achieve that clearance.

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