BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    PERIOTEST

    K Number: K872171 · Decision Jun 23, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    79
    Registration Numbers
    79
    Same Product Code
    85
    Applicant Total
    519
    Review Days
    15

    Basic Information

    Device Name
    PERIOTEST
    K Number
    K872171
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4200
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    SIEMENS MEDICAL SOLUTIONS USA, INC.
    Date Received
    June 8, 1987
    Decision Date
    June 23, 1987
    Product Code
    EKX
    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
    EKX Handpiece, Direct Drive, Ac-Powered

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