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510(k) Data Aggregation

    K Number
    K091972
    Date Cleared
    2009-09-23

    (84 days)

    Product Code
    Regulation Number
    870.1875
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Milscope Floating Mass Electronic Stethoscope, Model 300-01 is intended for medical diagnostic purposes only. It may be used for the detection and amplification of heart, lungs, arteries, veins, and other internal organs with the use of a selective frequency. It can be used on any person undergoing a physical assessment.

    Device Description

    Milscope Floating Mass Stethoscope

    AI/ML Overview

    The provided text is a 510(k) premarket notification letter from the FDA to Stethoscope Technologies, Inc. for their Milscope Floating Mass Electronic Stethoscope, Model 300-01.

    This document does not contain information regarding:

    • Acceptance criteria or reported device performance for a study.
    • Details about a study (sample size, data provenance, number/qualifications of experts, adjudication method).
    • Whether a multi-reader multi-case (MRMC) comparative effectiveness study was done, or an effect size.
    • Whether a standalone (algorithm only) performance study was done.
    • The type of ground truth used.
    • Sample size for a training set or how its ground truth was established.

    The document primarily states that the FDA found the device substantially equivalent to legally marketed predicate devices and that it can be marketed. It also includes the Indications for Use statement for the device.

    Therefore, I cannot fulfill your request for the detailed information about acceptance criteria and study design based on the provided input.

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