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510(k) Data Aggregation

    K Number
    K033734
    Date Cleared
    2003-12-17

    (19 days)

    Product Code
    Regulation Number
    862.2170
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    LIGHTCYCLER INSTRUMENT VERSION 1.2

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

    The LightCycler Instrument is a fully automated amplification and detection system for nucleic acids using fluorescence detection. The LightCycler is intended to be used by laboratory professionals trained in laboratory techniques and on the use of the analyzer.

    Device Description

    The LightCycler Instrument consists of a microvolume fluorimeter integrated with a thermal cycler. It combines rapid-cycler PCR in glass capillaries heated with hot-air with real-time fluorescence monitoring. The system is designed to reduce the time needed to achieve results from PCR and to enable the user to monitor the amplification of the PCR product simultaneously, in real-time and on-line.

    AI/ML Overview

    The provided text is a 510(k) summary for the LightCycler Instrument Version 1.2, which is an automated analyzer for nucleic acid amplification and detection. The core purpose of this document is to demonstrate "substantial equivalence" to a predicate device, the COBAS TaqMan Analyzer (K012966), rather than to present a study proving the device meets specific acceptance criteria through performance metrics.

    Therefore, many of the requested categories (acceptance criteria, reported device performance, sample size for test set, data provenance, number of experts, adjudication method, MRMC study, standalone study, type of ground truth, sample size for training set, and how ground truth was established for the training set) are not applicable or not explicitly detailed in this 510(k) summary.

    The document primarily focuses on comparing the features and intended use of the LightCycler Instrument to its predicate device to argue for substantial equivalence. It does not contain information about a prospective study with specific acceptance criteria and performance data for the LightCycler Instrument Version 1.2.

    However, based on the provided text, here's what can be extracted:

    1. A table of acceptance criteria and the reported device performance:
      • Acceptance Criteria: Not explicitly stated as pass/fail criteria for a new study. The acceptance is based on demonstrating "substantial equivalence" to the predicate device.
      • Reported Device Performance: While not acceptance criteria in the traditional sense of a performance study, the document reports technical specifications for the LightCycler Instrument that are compared to the predicate.
    FeatureLightCycler Reported Performance (as stated in comparison)Predicate (COBAS TaqMan Analyzer)
    Intended UseFully automated amplification and detection system for nucleic acids using fluorescence detection. Intended for laboratory professionals.Fully automated amplification and detection system for nucleic acids using 5' nuclease technology. Intended for laboratory professionals.
    Primary operational componentsIntegrated thermocycler and microvolume fluorimeter for walkaway PCR amplification and detectionIntegrated thermocycler and microvolume fluorimeter for walkaway PCR amplification and detection
    Detection ProcedureOptical detection of stimulated fluorescenceOptical detection of stimulated fluorescence
    Specimen typePurified nucleic acidsPurified nucleic acids
    Specimen PreparationPerformed off-linePerformed off-line
    Temperature range40 - 98 °C40 - 98 °C
    User interfacePC with instrument-specific software (LightCycler version 3.5 or higher)PC with instrument-specific software (Amplilink Software version 3.0 or higher)
    Heating method thermal cyclingHot air cycling with glass capillariesPeltier device with sample block
    Number of thermal cyclersOneFour
    Sample positions3296
    Sample Size10-20 uL in glass capillaries100 uL in 200 uL K-tubes
    Number of optical detection channelsThree with fixed wavelengths (530 nm, 640 nm, 710 nm)Four with wavelength ranges 510-710 nm
    Detection chemistryPaired hybridization probes using fluorescence resonance energy transfer (FRET)5' nuclease hydrolysis probes using FRET ('TaqMan technology')
    Detection timingDetection occurs at defined intervals during PCR cycle and can be viewed in real-timeDetection occurs only at end of each PCR cycle and can be viewed at completion of run
    Absolute temperature accuracy± 0.4 °C± 1.5 °C
    1. Sample size used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective):

      • Not applicable/Not provided. The document describes the device and compares its technical specifications to a predicate, but does not detail a specific performance study with a test set of samples.
    2. Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience):

      • Not applicable/Not provided. No human-expert-based ground truth establishment is mentioned as this is a device for nucleic acid analysis, not an imaging or diagnostic interpretation device.
    3. Adjudication method (e.g. 2+1, 3+1, none) for the test set:

      • Not applicable/Not provided.
    4. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance:

      • Not applicable. This device is a fully automated instrument for nucleic acid amplification and detection. It is not an AI-assisted diagnostic tool that aids human readers, and therefore, an MRMC study is not relevant here.
    5. If a standalone (i.e. algorithm only without human-in-the loop performance) was done:

      • The document describes the LightCycler Instrument as a "fully automated amplification and detection system," implying it operates in a standalone manner. However, no specific standalone performance study with detailed methodology and results is presented in this 510(k) summary; rather, its operational specifications are presented for comparison.
    6. The type of ground truth used (expert consensus, pathology, outcomes data, etc):

      • Not applicable/Not provided. For a device like this, the "ground truth" would typically refer to the known presence or absence of specific nucleic acid targets based on validated reference methods. This 510(k) summary does not contain details of such a validation study.
    7. The sample size for the training set:

      • Not applicable/Not provided. This document describes a physical instrument, not a machine learning algorithm that requires a training set.
    8. How the ground truth for the training set was established:

      • Not applicable/Not provided.
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