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510(k) Data Aggregation

    K Number
    K011865
    Manufacturer
    Date Cleared
    2001-07-31

    (47 days)

    Product Code
    Regulation Number
    870.1110
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ZOLL M SERIES IBP OPERATION; ZOLL M SERIES TEMPERATURE OPTION

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

    IBP: The ZOLL M Series IBP option is indicated for measuring arterial, venous, and intracranial pressures using invasive transducers with 5uV/V/mmHg sensitivity for use with resting patients in critical care and transport. The M Series IBP option is intended for use with adult and pediatric patients only. TEMPERATURE: The ZOLL M Series Temperature option is indicated for measuring temperature of adult and pediatric patients using YSI 400 compatible temperature sensors.

    Device Description

    ZOLL M Series IBP and Temperature Option

    AI/ML Overview

    I am sorry, but the provided text from the FDA 510(k) summary for the ZOLL M Series IBP and Temperature Options does not contain the acceptance criteria or a study detailing the device's performance against those criteria.

    The document is a clearance letter from the FDA, confirming that the device is substantially equivalent to legally marketed predicate devices. It outlines the indications for use and contraindications but does not include any technical specifications, performance metrics, or study results related to sensitivity, specificity, accuracy, or other performance characteristics.

    Therefore, I cannot provide the requested information in the table format or answer the questions about sample size, expert ground truth, adjudication methods, MRMC studies, standalone performance, or training set details. This information would typically be found in the more detailed 510(k) submission itself, which is not provided here.

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