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

    VIALOK SINGLE VIAL ACCESS DEVICE VENTED

    K Number: K122265 · Decision Aug 14, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    177
    Registration Numbers
    177
    Same Product Code
    205
    Applicant Total
    8
    Review Days
    15

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    Basic Information

    Device Name
    VIALOK SINGLE VIAL ACCESS DEVICE VENTED
    K Number
    K122265
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Yukon Medical, LLC
    Date Received
    July 30, 2012
    Decision Date
    August 14, 2012
    Product Code
    LHI
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    LHI Set, I.V. Fluid Transfer

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