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

    UMBILICAL CLAMP

    K Number: K915569 · Decision Sep 23, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    52
    Registration Numbers
    52
    Same Product Code
    35
    Applicant Total
    9
    Review Days
    286

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    Basic Information

    Device Name
    UMBILICAL CLAMP
    K Number
    K915569
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4530
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Gam Industries, Inc.
    Date Received
    December 12, 1991
    Decision Date
    September 23, 1992
    Product Code
    HFW
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HFW Clamp, Umbilical

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