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

    ReFlow System Mini

    K Number: K221918 · Decision Sep 29, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    68
    Registration Numbers
    69
    Same Product Code
    257
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    ReFlow System Mini
    K Number
    K221918
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.5550
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Anuncia Medical, Inc.
    Date Received
    July 1, 2022
    Decision Date
    September 29, 2022
    Product Code
    JXG
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JXG Shunt, Central Nervous System And Components

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    Other Clearances by Anuncia Medical, Inc.

    K Number Device Name
    K223603 Reflow System Mini and ReFlow Mini Flusher