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510(k) Data Aggregation

    K Number
    K013198
    Device Name
    FUJI VII CAPSULE
    Manufacturer
    Date Cleared
    2001-10-29

    (34 days)

    Product Code
    Regulation Number
    872.3275
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    FUJI VII CAPSULE

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

    GC Fuji VII is a capsulated restorative glass ionomer cement intended. for :

    • Treatment of early non-cavitated Icsions; such as tooth brush . abrasion and Root surface sensitivity.
    • Pit and Fissure Sealant .
    • · Intermediate restorative material
    • · Temporary filling of endodontic access
    Device Description

    GC Fuji VII is a capsulated restorative glass ionomer cement.

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for a dental device called "Fuji VII Capsule." This document does not contain information about acceptance criteria or a study proving the device meets those criteria.

    The letter explicitly states: "We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976..."

    This means the device was cleared based on substantial equivalence to a predicate device, not on a new study demonstrating its performance against specific acceptance criteria. The 510(k) pathway often relies on demonstrating that a new device is as safe and effective as a legally marketed predicate device, rather than requiring extensive new clinical trials with predefined acceptance criteria.

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