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

    RETRACTOR, SURGICAL

    K Number: K852330 · Decision Jun 27, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    658
    Registration Numbers
    658
    Same Product Code
    99
    Applicant Total
    8
    Review Days
    27

    Basic Information

    Device Name
    RETRACTOR, SURGICAL
    K Number
    K852330
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    SCHOLTEN SURGICAL INSTRUMENTS, INC.
    Date Received
    May 31, 1985
    Decision Date
    June 27, 1985
    Product Code
    GAD
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GAD Retractor

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