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510(k) Data Aggregation

    K Number
    K992404

    Validate with FDA (Live)

    Device Name
    THE WAND
    Manufacturer
    Date Cleared
    2000-06-06

    (323 days)

    Product Code
    Regulation Number
    880.5860
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    For injection of lidocaine subcutaneously or intramuscularly for infiltration and nerve block.

    Device Description

    The Wand™ is a computer controlled syringe consisting of a stationary motor housing which includes a metal piston whose speed of advance is regulated by a foot switch thus controlling the flow rate of anesthetic being injected. The device utilizes hypodermic needles and standard 1.8mm pre-filled carpules manufactured by various third parties. The anesthetic agent reaches the needle by means of a length of flexible vinyl tubing. The handpiece is made of rigid PVC. The holster containing the anesthetic carpule, the tubing and the handpiece are sold in a sterile condition as a disposable assembly for one-time use. The materials, principal of operation and intended use are the same as other marketed piston and cartridge syringes.

    AI/ML Overview

    The provided document is a 510(k) summary for "The Wand™ Syringe," which is a computer-controlled syringe for anesthetic delivery. This document focuses on demonstrating substantial equivalence to predicate devices and does not contain information about a formal study with acceptance criteria, sample sizes, expert ground truth, or adjudication methods for performance evaluation.

    Therefore, I cannot provide the requested information from the given text. The document's purpose is to clear the device for market based on its similarity to existing devices, not to present a detailed performance study against specific acceptance criteria.

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