Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K063390
    Date Cleared
    2007-03-01

    (112 days)

    Product Code
    Regulation Number
    862.1340
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    URINE CHEMISTRY ANALYZER UR-50

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

    Urine Chemistry Analyzer UR-50 is for use with the IND Urinalysis Reagent Strips for the determination of glucose, bilirubin, ketone, blood, protein, urobilinogen, nitrite, leukocytes, pH, and specific gravity in urine. It can be used for testing in the clinical laboratory setting. For professional use only. These measurements are useful in the evaluation of renal, urinary, and metabolic disorders.

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for the Urine Chemistry Analyzer UR-50. It does not contain any information about acceptance criteria or a study proving the device meets acceptance criteria.

    The document primarily focuses on:

    • The FDA's determination of substantial equivalence for the device to legally marketed predicate devices.
    • Regulatory classifications and requirements.
    • Contact information for further inquiries.
    • The intended use of the device, as described in the "Indications for Use" section.

    Therefore, I cannot fulfill your request for:

    1. A table of acceptance criteria and reported device performance.
    2. Sample sizes used for the test set or data provenance.
    3. Number of experts or their qualifications for ground truth.
    4. Adjudication method.
    5. MRMC comparative effectiveness study details.
    6. Standalone performance details.
    7. Type of ground truth used.
    8. Sample size for the training set.
    9. How ground truth for the training set was established.

    This information would typically be found in a separate submission document, such as the 510(k) summary or a detailed clinical study report, which is not part of the provided text.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1