BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    YOUNG D'GRANULATOR

    K Number: K932255 · Decision Apr 15, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    17
    Registration Numbers
    17
    Same Product Code
    8
    Applicant Total
    16
    Review Days
    340

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    Basic Information

    Device Name
    YOUNG D'GRANULATOR
    K Number
    K932255
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.4120
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Young Dental Manufacturing Co. 1, LLC
    Date Received
    May 10, 1993
    Decision Date
    April 15, 1994
    Product Code
    KMW
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    KMW Handpiece, Rotary Bone Cutting

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