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

    OVES CERVICAL CAP

    K Number: K993953 · Decision Mar 21, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    28
    Applicant Total
    1
    Review Days
    120

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    Basic Information

    Device Name
    OVES CERVICAL CAP
    K Number
    K993953
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.5250
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    Veos , Ltd.
    Date Received
    November 22, 1999
    Decision Date
    March 21, 2000
    Product Code
    HDR
    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
    HDR Cap, Cervical

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