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

    SCANLAN/TAHERI VALVULOTOME

    K Number: K911184 · Decision Feb 18, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    26
    Applicant Total
    19
    Review Days
    337

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    Basic Information

    Device Name
    SCANLAN/TAHERI VALVULOTOME
    K Number
    K911184
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4885
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Scanlan Intl., Inc.
    Date Received
    March 18, 1991
    Decision Date
    February 18, 1992
    Product Code
    MGZ
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MGZ Valvulotome

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