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

    B-WRAP

    K Number: K863777 · Decision Oct 24, 1986
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    28

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    Basic Information

    Device Name
    B-WRAP
    K Number
    K863777
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Bdf Plaza
    Date Received
    September 26, 1986
    Decision Date
    October 24, 1986
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N