BEUDAMED
    FDA 510(k) FDA unclassified Unknown 🇺🇸 United States

    Oasis Lacrimal Intubation Set

    K Number: K160710 · Decision May 13, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    20
    Registration Numbers
    21
    Same Product Code
    30
    Applicant Total
    1
    Review Days
    59

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    Basic Information

    Device Name
    Oasis Lacrimal Intubation Set
    K Number
    K160710
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Unknown
    Statement or Summary
    Summary
    Applicant
    Anodyne
    Date Received
    March 15, 2016
    Decision Date
    May 13, 2016
    Product Code
    OKS
    Advisory Committee
    Unknown
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

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

    Product Code Device Name
    OKS Lacrimal Stents And Intubation Sets

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