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

    MATERNITY SUPPORTER

    K Number: K770162 · Decision Feb 9, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    106
    Registration Numbers
    106
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    16

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    Basic Information

    Device Name
    MATERNITY SUPPORTER
    K Number
    K770162
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5160
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    R.G. Moore
    Date Received
    January 24, 1977
    Decision Date
    February 9, 1977
    Product Code
    FSD
    Advisory Committee
    General Hospital
    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
    FSD Binder, Abdominal

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