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

    PLACENTA AND OVUM FORCEPS

    K Number: K890386 · Decision Feb 13, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    41
    Registration Numbers
    41
    Same Product Code
    23
    Applicant Total
    63
    Review Days
    21

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    Basic Information

    Device Name
    PLACENTA AND OVUM FORCEPS
    K Number
    K890386
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4530
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Kinetic Medical Products
    Date Received
    January 23, 1989
    Decision Date
    February 13, 1989
    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

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    Other Clearances by Kinetic Medical Products

    K Number Device Name
    K890385 MIDWIFERY/OBSTETRICAL FORCEPS
    K890387 MALLEABLE PLACENTA CURETTE
    K890380 CERVICAL BIOPSY FORCEPS
    K890382 COMPRESSION FORCEPS
    K890376 VAGINAL SPECULUM
    K890383 HYSTERECTOMY FORCEPS
    K890216 MICROSURGICAL KERATOME
    K890378 UTERINE DRESSING FORCEPS
    K890379 UTERINE TENTACULUM
    K890389 UMBILICAL SCISSORS
    Search all 63 clearances from Kinetic Medical Products →