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

    MICROMAT W/VARIOUS MODELS

    K Number: K831117 · Decision May 30, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    1
    Applicant Total
    3
    Review Days
    421

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    Basic Information

    Device Name
    MICROMAT W/VARIOUS MODELS
    K Number
    K831117
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4370
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Pmt, Inc.
    Date Received
    April 5, 1983
    Decision Date
    May 30, 1984
    Product Code
    FNW
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FNW Pad, Kelly

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