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

    MODEL 116 FETAL MONITOR

    K Number: K891595 · Decision Jun 12, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    55
    Registration Numbers
    55
    Same Product Code
    213
    Applicant Total
    136
    Review Days
    84

    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
    MODEL 116 FETAL MONITOR
    K Number
    K891595
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.2740
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Ge Medical Systems Information Technologies
    Date Received
    March 20, 1989
    Decision Date
    June 12, 1989
    Product Code
    HGM
    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
    HGM System, Monitoring, Perinatal

    Similar 510(k) Clearances

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

    ANNE Maternal

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

    Sonicaid Team3

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

    Fetal & Maternal Monitor (F15A, F15A Air)

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

    Sonicaid Team3

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

    PeriCALM Patterns 3.0

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

    Avalon CL Fetal & Maternal (F&M) Pod (866488), Avalon CL Fetal & Maternal (F&M) Patch (989803196341)

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

    Other Clearances by Ge Medical Systems Information Technologies

    K Number Device Name
    K120770 QT GUARD PLUS ANALYSIS SYSTEM
    K102426 CARESCAPE MODEL V100 VITAL SIGNS MONITOR
    K092369 12SL ECG ANALYSIS PROGRAM
    K093141 MARS HOLTER ANALYSIS WORKSTATION
    K092027 CARESCAPE MONITOR B850
    K090702 MODIFICATION TO DASH 2500 PATIENT MONITOR
    K083750 CAPNOSTAT / CAPNOFLEX CO2 SYSTEM
    K083639 MUSE CARDIOLOGY INFORMATION SYSTEM WITH VMWARE
    K082851 MULTLINK CABLE AND LEADWIRE SYSTEM
    K081437 MAC 1600 ECG ANALYSIS SYSTEM
    Search all 136 clearances from Ge Medical Systems Information Technologies →