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510(k) Data Aggregation

    K Number
    K062158
    Device Name
    LC SPRINT STAR
    Date Cleared
    2006-08-28

    (31 days)

    Product Code
    Regulation Number
    868.5630
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    LC SPRINT STAR

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

    The LC Sprint Star is a handheld nebulizer, designed to aerosolize medication approved for nebulization and prescribed by a physician. The LC Sprint Star is intended for pediatric and adult patients consistent with the indications for the aerosol medication.

    Device Description

    The LC Sprint Star is a small, single patient use, reusable air-powered nebulizer for the inhalation treatment of aerosolized medications. The device is non-sterile, prescriptionuse only, intended for use in hospital, clinic, or home environments.

    LC Sprint Star is a cosmetically and geometrically modified version of the LC Sprint nebulizer currently marketed by PARI. The LC Sprint Star has an inspiratory balve on the top component and an expiratory valve on the mouthpiece, allowing for breathcontrolled aerosol output.

    The LC Sprint Star will be available as a stand-alone item or a configuration component containing:

    • LC Sprint Star nebulizer (consisting of nebulizer cup, top, and baffle insert) I
    • L Mouthpiece
    • Oxygen tubing (optional) 트
    • 트 Mask (optional)
    AI/ML Overview

    The provided text describes a 510(k) submission for a nebulizer, not an AI/ML device. Therefore, the requested information regarding acceptance criteria and studies for an AI/ML device cannot be extracted from this document, as it does not pertain to such a device.

    The document discusses the LC Sprint Star Reusable Nebulizer, comparing it to predicate devices and detailing its indications for use. It's a medical device clearance, not an AI/ML product.

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