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

    OVA1 Next Generation

    K Number: K150588 · Decision Mar 18, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    5
    Applicant Total
    1
    Review Days
    375

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    Basic Information

    Device Name
    OVA1 Next Generation
    K Number
    K150588
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.6050
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Vermillion, Inc.
    Date Received
    March 9, 2015
    Decision Date
    March 18, 2016
    Product Code
    ONX
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    IM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    ONX Ovarian Adnexal Mass Assessment Score Test System

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