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510(k) Data Aggregation

    K Number
    K964738
    Device Name
    ELPHA 2000 CONTI
    Manufacturer
    Date Cleared
    1997-08-14

    (274 days)

    Product Code
    Regulation Number
    876.5320
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ELPHA 2000 CONTI

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

    Electrical stimulation of the pelvic floor muscles with the use of vaginal probe. The effect is strengthening the pelvic floor muscles and an activation of the central nervous system.

    Electrical stimulation of the pelvic floor muscles can reduce urinary incontinence among stress and urge incontinent adult females.

    Device Description

    Not Found

    AI/ML Overview

    The provided FDA 510(k) clearance letter and Indications for Use statement for the "Elpha 2000 CONTI" device do not contain information about acceptance criteria or a study demonstrating device performance.

    Therefore, I cannot provide the requested information, including:

    1. A table of acceptance criteria and the reported device performance.
    2. Sample size used for the test set and data provenance.
    3. Number of experts used to establish ground truth and their qualifications.
    4. Adjudication method for the test set.
    5. If a multi reader multi case (MRMC) comparative effectiveness study was done.
    6. If a standalone (algorithm only) performance study was done.
    7. The type of ground truth used.
    8. The sample size for the training set.
    9. How the ground truth for the training set was established.

    This document is primarily a clearance letter affirming substantial equivalence to a predicate device for specific indications of use, rather than a detailed report of a performance study.

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