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510(k) Data Aggregation

    K Number
    K990587
    Manufacturer
    Date Cleared
    1999-04-07

    (43 days)

    Product Code
    Regulation Number
    866.5775
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Abbott Liquid RF Control is intended for use as a quality control serum to monitor the precision of laboratory testing procedures for the analytes listed in the value sheet.

    Device Description

    Abbott Liquid RF Control

    AI/ML Overview

    This is an FDA Premarket Notification (510(k)) letter for the Abbott Liquid RF Control, a quality control serum. The letter itself does not contain the detailed study information you are requesting. It primarily states that the device is substantially equivalent to a legally marketed predicate device and can therefore be marketed.

    To answer your specific questions about acceptance criteria and study details, I would need to review the actual 510(k) submission document or a summary of its contents, which typically includes performance data. The provided text is only the FDA's regulatory response letter.

    Therefore, I cannot provide the requested information based solely on the text provided. The document you've shared discusses the regulatory approval of a device, not the technical details of the studies performed to achieve that approval.

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