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

    ILC FORCEPS PADS

    K Number: K905583 · Decision Apr 12, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    62
    Registration Numbers
    62
    Same Product Code
    9
    Applicant Total
    6
    Review Days
    121

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    Basic Information

    Device Name
    ILC FORCEPS PADS
    K Number
    K905583
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4400
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Inman Liebelt Corp.
    Date Received
    December 12, 1990
    Decision Date
    April 12, 1991
    Product Code
    HDA
    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
    HDA Forceps, Obstetrical

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