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510(k) Data Aggregation

    K Number
    K012761
    Date Cleared
    2001-11-01

    (76 days)

    Product Code
    Regulation Number
    872.3765
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    PRIME-DENT VISIBLE LIGHT CURE PIT & FISSURE SEALANT

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

    Prime-Dent® Visible Light Cure Pit & Fissure Sealant (opaque and clear) is a BisGMA based visible light cured resin for the sealing of deciduos teeth and the filling of fissures in primary tooth structure.

    Device Description

    Not Found

    AI/ML Overview

    This is an FDA Premarket Notification (510(k)) for a dental sealant. This type of document declares "substantial equivalence" to a predicate device, meaning it's similar enough that it doesn't require new clinical trials like a premarket approval (PMA) would. Therefore, the document does not contain information about acceptance criteria or a study proving the device meets them.

    The FDA letter explicitly states: "We have reviewed your Section 510(k) premarket notification... and have determined the device is substantially equivalent... to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976... You may, therefore, market the device..."

    To answer the requested questions, one would need different documentation, such as a PMA submission or a clinical study report for a novel device.

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