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510(k) Data Aggregation

    K Number
    K971225
    Date Cleared
    1997-07-17

    (106 days)

    Product Code
    Regulation Number
    864.7290
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    CRYO CHECK FACTOR VIII DEFICIENT PLASMA

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

    CryoCheck Factor VIII Deficient Plasma is human plasma deficient in the factor VIII coagulation protein while having all other coagulation factors within normal limits. It is indicated for use to assess factor VIII deficiencies in in vitro clotbased factor VIII assays using the activated partial thromboplastin time.

    Device Description

    CryoCheck Factor VIII Deficient Plasma is human plasma deficient in the factor VIII coagulation protein while having all other coagulation factors within normal limits.

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for a device called "CryoCheck Factor VIII Deficient Plasma." This document does not contain any information about acceptance criteria, device performance, study details, or ground truth establishment relevant to an AI/ML device.

    The letter is a regulatory approval for an in vitro diagnostic product, not a software device, and primarily states that the device is substantially equivalent to existing devices. Therefore, I cannot extract the requested information regarding acceptance criteria, study details, or AI/ML specific metrics.

    To provide the requested information, a different type of document, such as a clinical study report, a performance evaluation report, or a 510(k) summary for an AI/ML device, would be necessary.

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