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510(k) Data Aggregation

    K Number
    K052838
    Manufacturer
    Date Cleared
    2005-11-09

    (33 days)

    Product Code
    Regulation Number
    864.8625
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    LIQUICHEK DIABETES CONTROL, LEVEL 1,2,3,4

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

    Liquichek Diabetes Control is intended for use as an assayed quality control material to monitor the precision of laboratory testing procedures for the analytes listed in the package insert.

    Device Description

    This is a liquid product prepared from human whole blood containing preservatives and stabilizers.

    AI/ML Overview
    1. Table of Acceptance Criteria and Reported Device Performance:

      Acceptance CriteriaReported Device Performance
      Open vial Stability: 14 days at 2°C to 8°C14 days at 2°C to 8°C
      Shelf Life: 3 years at -10°C to -70°C or 6 months when stored tightly capped at 2°C to 8°C3 years at -10°C to -70°C or 6 months when stored tightly capped at 2°C to 8°C
    2. Sample Size for the Test Set and Data Provenance:
      The document does not explicitly state the sample size used for the stability studies. The data provenance is "retained on file at Bio-Rad Laboratories," indicating it is internal company data, likely retrospective.

    3. Number of Experts Used to Establish Ground Truth and Qualifications:
      Not applicable. This device is a quality control material, and its performance is assessed against predefined stability parameters, not through expert interpretation of data.

    4. Adjudication Method for the Test Set:
      Not applicable. The stability studies involve quantitative measurements against established criteria, not subjective expert review.

    5. MRMC Comparative Effectiveness Study:
      Not applicable. This is a quality control material, not a diagnostic device that assists human readers.

    6. Standalone Performance:
      Yes, the reported performance is for the device standalone, as a quality control material. Its stability characteristics are assessed independently.

    7. Type of Ground Truth Used:
      The ground truth is established based on the intrinsic chemical and physical stability properties of the control material under specified storage conditions. This would typically involve laboratory measurements over time to assess the integrity and performance of the analytes within the control.

    8. Sample Size for the Training Set:
      Not applicable. This device is a quality control material, not an AI/ML model that requires a training set.

    9. How Ground Truth for the Training Set Was Established:
      Not applicable. As noted above, this device does not involve a training set.

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