BEUDAMED
    FDA 510(k) Substantially Equivalent 🇬🇧 United Kingdom

    FLEXISTAND MAJOR

    K Number: K852152 · Decision Nov 5, 1985
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    172

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    Basic Information

    Device Name
    FLEXISTAND MAJOR
    K Number
    K852152
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Zygotek Assoc.
    Date Received
    May 17, 1985
    Decision Date
    November 5, 1985
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N