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510(k) Data Aggregation

    K Number
    K240696
    Date Cleared
    2024-06-14

    (92 days)

    Product Code
    Regulation Number
    880.5045
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    Airdog X8 Air Purifier (KJ800F-X8)

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

    The Airdog X8 Air Purifier is a mobile air cleaner intended to remove particles from the air for medical purposes. The device is intended for indoor use only. The Airdog X8 has been demonstrated to effectively inactivate H3N2 and reduce Staphylococcus albus by 4 log with L5 speed.

    Device Description

    The Airdog X8 Air Purifier (X8) is a mobile air cleaner. The air from the room enters the X8 and passes a pre-filter, ionization frame, ionization field, collecting plates and carbon filter that captures particular matter and biological agents from the air. The X8 contains multiple PCB modules, device status indicators, power switch and a display panel, it allows user to select between different operation parameters, including auto-mode, sleep mode and wind speed. The Ionization wireframe and the collecting plate can be cleaned routinely and are reusable. X8 is powered from an AC wall outlet. It is intended to be used indoors only. The device is not intended to be connected to other instruments or medical devices.

    AI/ML Overview

    The provided text is a 510(k) Summary for the Airdog X8 Air Purifier. It lacks the details typically found in a study proving a device meets specific acceptance criteria, especially for an AI/ML-driven device with complex performance metrics like those involving human readers or expert consensus. This document pertains to an air purifier, and its "performance data" is focused on physical and biological filtration capabilities, not on an AI's diagnostic or assistive accuracy.

    Therefore, I cannot extract information related to:

    • Sample size used for the test set and data provenance (e.g., country of origin, retrospective/prospective)
    • Number of experts used to establish ground truth and their qualifications
    • Adjudication method for the test set
    • Multi-Reader Multi-Case (MRMC) comparative effectiveness study or effect size
    • Standalone (algorithm only) performance
    • Type of ground truth used (expert consensus, pathology, outcomes data)
    • Sample size for the training set
    • How ground truth for the training set was established

    However, based on the provided text, I can infer the "acceptance criteria" and "reported device performance" related to the air purifier's function.

    Here's a breakdown of what can be extracted:

    1. A table of acceptance criteria and the reported device performance

    While not explicitly called "acceptance criteria" with pass/fail thresholds in the typical AI/ML sense, the document lists specifications and test results that serve as performance benchmarks.

    Acceptance Criteria (Implied)Reported Device Performance
    Biological Agent Reduction (H3N2 Influenza virus)99.99% reduction with L5 speed operation (Airdog X8)
    Biological Agent Reduction (Staphylococcus albus)4 log reduction with L5 speed (Airdog X8)
    Particle Filtration (PM2.5)4-log reduction in PM2.5 particles in 120 minutes in a 30m³ chamber (Airdog X8)
    Ozone EmissionMeets the requirements of UL867 (
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