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

    MR. RAZOR II TWIN

    K Number: K882388 · Decision Jul 13, 1988
    View on FDA
    Classifications
    0
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    80
    Applicant Total
    1
    Review Days
    33

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    Basic Information

    Device Name
    MR. RAZOR II TWIN
    K Number
    K882388
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Burney Products Corp.
    Date Received
    June 10, 1988
    Decision Date
    July 13, 1988
    Product Code
    LDQ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    SU
    Third Party
    N

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