BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    DISPOSABLE VACUUM CURETTE

    K Number: K790032 · Decision Feb 1, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    129
    Registration Numbers
    129
    Same Product Code
    10
    Applicant Total
    2
    Review Days
    29

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    Basic Information

    Device Name
    DISPOSABLE VACUUM CURETTE
    K Number
    K790032
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    884.4530
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    British Marketing Ent., Ltd.
    Date Received
    January 3, 1979
    Decision Date
    February 1, 1979
    Product Code
    HCY
    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
    HCY Curette, Uterine

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