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510(k) Data Aggregation

    K Number
    K983578
    Manufacturer
    Date Cleared
    1998-11-12

    (30 days)

    Product Code
    Regulation Number
    862.1660
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Architect Testosterone MasterCheck is intended for use in the verification of sensitivity, calibration linearity, and reportable range on the Abbott Architect i System

    Device Description

    Architect Testosterone MasterCheck Level 0 contains bovine serum Architect Testosterone MasterCheck Levels 1, 2 and 3 contain testosterone prepared in bovine serum. Preservative: Antimicrobial agent.

    AI/ML Overview

    The provided document is a 510(k) summary for a medical device called "Architect Testosterone MasterCheck." This document focuses on establishing substantial equivalence to a predicate device and does not contain detailed information about specific acceptance criteria or a study that rigorously proves the device meets such criteria in terms of analytical performance.

    Instead, the document primarily addresses:

    • Device Description: What the Architect Testosterone MasterCheck is (bovine serum with testosterone).
    • Intended Use: Verification of sensitivity, calibration linearity, and reportable range on the Abbott Architect i System.
    • Substantial Equivalence Comparison: A table comparing its characteristics (intended use, form, matrix, storage, analytes, open vial claim) to a predicate device (Casco Standards Document Serum Multi-Analyte Verification Test Set).
    • Regulatory Classification: Class I device.
    • FDA Clearance: Notification of clearance for marketing based on substantial equivalence.

    Therefore, it is not possible to provide the requested information regarding acceptance criteria, device performance, sample sizes for test/training sets, expert qualifications, adjudication methods, MRMC studies, or standalone performance, as this type of information is not present in the provided 510(k) summary.

    In summary, the document does not contain the information needed to answer the questions about acceptance criteria and a study proving device performance.

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