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510(k) Data Aggregation

    K Number
    K041410
    Manufacturer
    Date Cleared
    2004-07-28

    (62 days)

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

    PUNCTUR-GUARD WINGED SET FOR BLOOD COLLECTION, MODEL 5118

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

    The intended use of the device is to inject fluids into, or withdraw fluids from, parts of body below the surface of the skin.

    Device Description

    The PUNTUR-GUARD protects the health care worker from accidental needlestick by providing a blunting that renders safe the needle once it has entered the patient's vein. The PUNCTUR-GUARD is intended to enhance current safety needle programs

    AI/ML Overview

    The provided text is a 510(k) premarket notification approval letter for the PUNCTUR-GUARD® Winged Set for Blood Collection and Intravenous Infusion. This document does not contain any information regarding acceptance criteria or a study proving that the device meets such criteria.

    The letter from the FDA confirms that the device is substantially equivalent to legally marketed predicate devices. This determination is based on the information submitted in the 510(k) application, which typically includes device description, indications for use, comparison to predicates, and sometimes performance data if necessary to establish substantial equivalence. However, the details of any performance studies, acceptance criteria, or their results are not present within this specific document.

    Therefore, I cannot provide the requested information. The document focuses on regulatory approval rather than a detailed technical report of device performance and testing.

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