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510(k) Data Aggregation

    K Number
    K022682
    Date Cleared
    2002-11-05

    (85 days)

    Product Code
    Regulation Number
    862.1150
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    RANDOX C-REACTIVE PROTEIN CALIBRATOR

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

    The Randox Laboratories Limited C-Reactive Protein Calibrators are liquid calibrators containing human recombinant CRP in a stabilised protein matrix. They have been developed for use in the calibration of CRP assays. The constituent concentrations of the Randox Laboratories Limited C-Reactive Protein Calibrator are present at 6 levels.

    The Randox Laboratories Limited C-Reactive Protein Calibrators should only be used by suitably qualified laboratory personnel under appropriate laboratory conditions.

    Device Description

    The Randox Laboratories Limited C-Reactive Protein Calibrators are liquid calibrators containing human recombinant CRP in a stabilised protein matrix. They have been developed for use in the calibration of CRP assays. The constituent concentrations of the Randox Laboratories Limited C-Reactive Protein Calibrator are present at 6 levels.

    AI/ML Overview

    The provided document is a 510(k) premarket notification letter from the FDA to Randox Laboratories Limited regarding their C-Reactive Protein Calibrator. It states that the device is substantially equivalent to legally marketed predicate devices.

    However, the document does not contain any information regarding acceptance criteria, device performance studies, sample sizes, ground truth establishment, or expert involvement. The letter is an administrative approval, confirming that the device can be marketed based on its substantial equivalence to existing products, but it does not detail the technical studies that would typically be performed to establish performance against acceptance criteria.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets them using the provided text.

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