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

    LAPAROSCOPIC FORCEPS

    K Number: K911474 · Decision Jul 3, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    41
    Registration Numbers
    41
    Same Product Code
    23
    Applicant Total
    94
    Review Days
    90

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    LAPAROSCOPIC FORCEPS
    K Number
    K911474
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4530
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    United States Endoscopy Group, Inc.
    Date Received
    April 4, 1991
    Decision Date
    July 3, 1991
    Product Code
    HCZ
    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
    HCZ Forceps, Surgical, Gynecological

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (HCZ), ordered by most recent decision date.

    Fetzer Medical Gynecological Forceps

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    JARIT GYNECOLOGICAL FORCEPS, MILTEX GYNECOLOGICAL FORCEPS, MEISTERHAND GYNECOLOICAL FORCEPS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    FORCEPS, SURGICAL GYNECOLOGICAL

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PEARL PACKING FORCEPS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HYSTERECTOMY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology
    View all

    Other Clearances by United States Endoscopy Group, Inc.

    K Number Device Name
    K192265 gi-4000 Electrosurgical Generator
    K200745 Lariat, Hot/Cold Snare
    K192059 Bio Guard Air/Water & Suction Valves
    K191559 AquaShield System CO2, AquaShield System CO2-PENTAX, AquaShield System CO2-FUJIFILM
    K182909 Roth Net Retriever Product Line
    K182258 AquaShield System CO2 ; AquaShield System CO2 - PENTAX ; AquaShield System CO2 - Fujifilm
    K173650 AquaShield System CO2- Fujifilm
    K172805 gi-4000 Electrosurgical Generator
    K163495 AdvanCE capsule endoscope delivery device
    K163492 Oracle EUS Balloon; Oracle EUS latex balloon - Olympus Radial; Oracle EUS latex balloon - Olympus Linear; Oracle EUS latex balloon - Fujinon Radial; Oracle EUS latex balloon - Fujinon Linear
    Search all 94 clearances from United States Endoscopy Group, Inc. →