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510(k) Data Aggregation

    K Number
    K013263
    Date Cleared
    2002-07-29

    (301 days)

    Product Code
    Regulation Number
    866.5100
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    FRED HUTCHINSON CANCER RESEARCH CENTER ENZYME ANTI-SR PROTEIN ANTIBODY TEST

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

    The Fred Hutchinson Cancer Research Center Anti-SR test is an enzyme immunoassay (EIA) for the detection and semiquantitative measure of human antibodies against a type of ribonucleoproteins (RNPs) called SR Proteins. The test is intended as an aid in the diagnosis of Systemic Lupus Erythematosis (SLE) .

    Device Description

    The Fred Hutchinson Cancer Research Center Anti-SR test is an enzyme immunoassay (EIA) for the detection and semiquantitative measure of human antibodies against a type of ribonucleoproteins (RNPs) called SR Proteins.

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for a device called "FHCRC Anti-SR Test." This letter grants clearance based on substantial equivalence to a predicate device, but it does not contain the detailed study information, acceptance criteria, or performance data that would be found in a 510(k) submission document itself.

    Therefore,Based on the provided document, I cannot extract the acceptance criteria or a study proving the device meets those criteria. The document is solely an FDA clearance letter, which references a 510(k) premarket notification but does not contain the specifics of that submission.

    Here's why the requested information cannot be found in the provided text:

    • No Acceptance Criteria or Performance Data: The letter states the device is "substantially equivalent" to a predicate device but does not detail the specific performance metrics (like sensitivity, specificity, accuracy) or the thresholds for those metrics that would constitute "acceptance criteria."
    • No Description of a Study: While a study would have been part of the 510(k) submission that led to this letter, the letter itself does not describe the study design, sample sizes, ground truth establishment, or expert qualifications.

    The letter explicitly mentions:

    • Trade/Device Name: Fred Hutchinson Cancer Research Center (FHCRC) Anti-SR Test
    • Regulation Name: Antinuclear Antibody Immunological Test System
    • Indications For Use: An enzyme immunoassay (EIA) for the detection and semiquantitative measure of human antibodies against SR Proteins, intended as an aid in the diagnosis of Systemic Lupus Erythematosis (SLE).

    To answer your request, one would need access to the original 510(k) submission for device K013263.

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