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510(k) Data Aggregation

    K Number
    K962799
    Manufacturer
    Date Cleared
    1996-10-11

    (85 days)

    Product Code
    Regulation Number
    876.1500
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Applicant Name (Manufacturer) :

    RICHARD WOLF GMBH

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

    The Miniature Laparoscope Set is used to apply and maintain pneumoperitoneum in the usual way, and to introduce telescopes and other auxiliary instruments, such as forceps and scissors for diagnostic and therapeutic purposes.

    Device Description

    Cannula and tubes are made of medical grade stainless steel and chrome plated brass.

    Telescopes are made of medical grade stainless steel (sleeve), glass-lenses, glassfibers, brass chrome plated (housing) and plastic (eyepiece).

    AI/ML Overview

    The provided text is a 510(k) Summary of Safety and Effectiveness for a medical device (Mini Laparoscopes). It describes the device, its intended use, and argues for its equivalence to existing devices. However, the document does not contain any information regarding specific acceptance criteria, a study proving the device meets acceptance criteria, or any of the detailed AI-related study design elements (sample sizes, expert qualifications, adjudication, MRMC, standalone performance, training set details) requested in your prompt.

    The "Performance Data" section explicitly states: "Instruments have been tested to assure the function of the spring loaded cannula and the possibility of steam autoclaving." This refers to basic functional testing, not a clinical study to establish performance against acceptance criteria in the way you've described for AI models. The "Clinical Tests" section explicitly states: "No clinical tests performed."

    Therefore, I cannot fulfill your request to describe the acceptance criteria and study as the provided text does not contain this information.

    Missing Information:

    • Table of acceptance criteria and reported device performance: Not present.
    • Sample size used for the test set and data provenance: Not applicable as no clinical test set is mentioned.
    • Number of experts used to establish the ground truth...: Not applicable.
    • Adjudication method: Not applicable.
    • Multi reader multi case (MRMC) comparative effectiveness study: Not applicable.
    • Standalone (algorithm only) performance: Not applicable.
    • Type of ground truth used: Not applicable.
    • Sample size for the training set: Not applicable.
    • How the ground truth for the training set was established: Not applicable.
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