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510(k) Data Aggregation

    K Number
    K072919
    Manufacturer
    Date Cleared
    2007-11-02

    (18 days)

    Product Code
    Regulation Number
    870.1425
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The VENDYS Model 6000 Model B/BC is a non-invasive digital temperature monitoring device. The device provides continuous monitoring of body surface temperature at multiple sites simultaneously (e.g. fingertips on the study and control hands). It is intended to use for measurement of vascular reactivity by monitoring temperature changes before, during, and after a reactive hyperemia test using a 2-5 minute cuff occlusion procedure.

    Device Description

    The VENDYS Model 6000 Model B/BC is a non-invasive digital temperature monitoring device. The device provides continuous monitoring of body surface temperature at multiple sites simultaneously (e.g. fingertips on the study and control hands).

    AI/ML Overview

    The provided document is a 510(k) clearance letter from the FDA for the VENDYS Model 6000 B B/C device. It does not contain specific information regarding acceptance criteria, device performance studies, sample sizes, ground truth establishment, or expert qualifications as requested.

    The letter acknowledges the substantial equivalence of the device to a legally marketed predicate device but does not detail the technical performance data or the studies conducted to demonstrate that performance. Therefore, I cannot provide a table of acceptance criteria and reported device performance or other specific study details based on this document.

    To answer your request, I would need access to the actual 510(k) submission, which would include the performance data and study reports.

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