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

    GDT-1000 System

    K Number: K180096 · Decision Apr 16, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    135
    Registration Numbers
    135
    Same Product Code
    170
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    GDT-1000 System
    K Number
    K180096
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1690
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Acuvu, Inc.
    Date Received
    January 16, 2018
    Decision Date
    April 16, 2018
    Product Code
    HIH
    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
    HIH Hysteroscope (And Accessories)

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    Other Clearances by Acuvu, Inc.

    K Number Device Name
    K211227 HTx Disposable Hysteroscope System