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

    IMAX PERIOTIPS

    K Number: K851841 · Decision May 29, 1985
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    33

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    Basic Information

    Device Name
    IMAX PERIOTIPS
    K Number
    K851841
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Stram Dental, Inc.
    Date Received
    April 26, 1985
    Decision Date
    May 29, 1985
    Advisory Committee
    Unknown
    Review Advisory Committee
    DE
    Third Party
    N