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510(k) Data Aggregation

    K Number
    K022862
    Device Name
    TRANSCURE, MODEL 2910
    Manufacturer
    KINETIC INSTRUMENTS, INC.
    Date Cleared
    2002-10-18

    (51 days)

    Product Code
    EBZ
    Regulation Number
    872.6070
    Why did this record match?
    Applicant Name (Manufacturer) :

    KINETIC INSTRUMENTS, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Light Activation System for Dental Restorative Resins Visible Inspection of the Oral Cavity
    Device Description
    Not Found
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    K Number
    K012946
    Device Name
    SUNLITELED MODEL #2810
    Manufacturer
    KINETIC INSTRUMENTS, INC.
    Date Cleared
    2001-10-02

    (28 days)

    Product Code
    EBZ
    Regulation Number
    872.6070
    Why did this record match?
    Applicant Name (Manufacturer) :

    KINETIC INSTRUMENTS, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Light Activation System for Dental Restorative Resins
    Device Description
    SunliteLED Model #2810
    Ask a Question

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