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510(k) Data Aggregation

    K Number
    K092025
    Manufacturer
    Date Cleared
    2011-01-27

    (570 days)

    Product Code
    Regulation Number
    872.5550
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    FLUID FILLED TEETHER - GEL

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

    All teethers instruct consumer to: .

    • Clean before use with a damp cloth and mild soap. Air dry. o
    • o Not dishwasher safe
    • Freezer safe ◆

    Teether acts as an aid in relieving an infant's gums due to teething. .

    Device Description

    Fluid Filled Teether - Gel

    AI/ML Overview

    I am sorry, but the provided text does not contain information about the acceptance criteria and study proving device performance as requested. The document is an FDA 510(k) clearance letter for a "Fluid Filled Teether - Gel" (K092025), which indicates that the device is substantially equivalent to legally marketed predicate devices. It discusses regulatory classification, general controls, and compliance requirements.

    However, it does not include:

    1. A table of acceptance criteria and reported device performance.
    2. Details about sample sizes for test sets, data provenance, or retrospective/prospective nature.
    3. Information on the number or qualifications of experts used to establish ground truth.
    4. Adjudication methods.
    5. Multi-reader multi-case (MRMC) comparative effectiveness studies or effect sizes.
    6. Standalone algorithm performance.
    7. The type of ground truth used (e.g., pathology, outcomes data).
    8. Sample size for the training set.
    9. How ground truth for the training set was established.

    This document is a regulatory approval, not a technical study report detailing performance metrics and study methodologies.

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