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510(k) Data Aggregation

    K Number
    K021565
    Date Cleared
    2002-11-14

    (185 days)

    Product Code
    Regulation Number
    880.5440
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    LUTHER SAFETY HUBER NEEDLE SET

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

    The Luther Safety Huber Needle Set is a device intended to administer drugs to a patient from a container through a subcutaneous implanted port. The Huber Needle safety needle cover is manually activated. When the safety feature is activated, the device is designed to aid in the prevention of accidental needle sticks.

    Device Description

    The Luther Safety Huber Needle Set is a standard right angle Huber needle and administration set with a needlestick prevention feature, designed for use with a vascular access infusion system. It is manufactured with conventional medical grade, biocompatible materials. The Luther Safety Huber Needle Set operates as a standard Huber needle with the addition of a safety feature to aid in the prevention of needlestick injuries to the health practitioner. It is supplied sterile for single use only.

    AI/ML Overview

    Here's an analysis of the provided text regarding the acceptance criteria and study for the Luther Safety Huber Needle Set:

    1. Table of Acceptance Criteria and Reported Device Performance

    Acceptance Criteria (Implied)Reported Device Performance
    Prevention of sharps injuryNo incidences of sharps injury
    Safety feature activationNo incidences where the safety feature failed to activate

    2. Sample Size and Data Provenance

    • Test Set Sample Size: 692 Luther Safety Huber Needle Sets.
    • Data Provenance: The study was a "simulated use clinical trial," which generally implies a prospective study. The document does not specify the country of origin of the data.

    3. Number of Experts Used to Establish Ground Truth and Qualifications

    The document does not mention the use of experts to establish ground truth for this particular study. The assessment of sharps injuries and safety feature activation appears to be directly observed outcomes from the simulated use.

    4. Adjudication Method

    The document does not describe any adjudication method. Given the nature of the observed outcomes (sharps injury, safety feature activation), direct observation likely formed the basis of the data collection.

    5. Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study

    No MRMC comparative effectiveness study was done. This type of study is more common for diagnostic imaging devices where human interpretation is a key component. The Luther Safety Huber Needle Set is a medical device designed for drug administration and sharps injury prevention.

    6. Standalone (Algorithm Only) Performance Study

    No standalone performance study was done. This device does not involve an algorithm. Its function is mechanical/physical, relying on a safety feature to prevent needle sticks.

    7. Type of Ground Truth Used

    The ground truth used was direct observation of outcomes in a simulated use clinical trial:

    • Presence/absence of sharps injuries.
    • Successful/unsuccessful activation of the safety feature.

    8. Sample Size for the Training Set

    Not applicable. This device does not use machine learning or algorithms that require a training set.

    9. How the Ground Truth for the Training Set Was Established

    Not applicable, as there is no training set for this type of device.

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