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

    FORCEPS, OB, NON-COMPRESSIVE

    K Number: K771106 · Decision Jul 1, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    65
    Registration Numbers
    65
    Same Product Code
    9
    Applicant Total
    1
    Review Days
    11

    Basic Information

    Device Name
    FORCEPS, OB, NON-COMPRESSIVE
    K Number
    K771106
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4400
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    ZEPPELIN MEDIZINLECHNIK GMBH
    Date Received
    June 20, 1977
    Decision Date
    July 1, 1977
    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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