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510(k) Data Aggregation

    K Number
    K082212
    Date Cleared
    2009-01-22

    (169 days)

    Product Code
    Regulation Number
    870.1650
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    SYRINGE WITH HANDI-FIL

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

    The Syringe with Handi-Fil is part of the contrast delivery system which is designed to mject radiopaque contrast media and/or salıne into the vascular system for Angiographic or CT procedures as prescribed by qualified healthcare professionals

    Device Description

    The proposed device is a disposable, single-use syringe, used to deliver radiographic contrast media and/or salme into a patient's vascular system for the purpose of obtaming enhanced diagnostic images The Syringe with Handi-Fil is plastic and consists of the same components as the predicate device The configuration is equivalent to other syringes already marketed by Mallinckrodt The synnge is provided to the customer packaged and sterilized. This submission covers the following devices: 150 ml syringe with Handı-Fil, 200 ml syringe with Handı-Fil.

    AI/ML Overview

    I am sorry, but based on the provided text, there is no information about acceptance criteria, device performance tables, study designs (sample sizes, data provenance, expert panels, adjudication methods, MRMC studies, standalone studies), or ground truth establishment. The document is a 510(k) summary for a medical device (Syringe with Handi-Fil) establishing substantial equivalence to a predicate device. It focuses on device description, intended use, and a comparison of features, not on the results of a performance study.

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