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

    Accuryn Monitoring System

    K Number: K153655 · Decision Apr 15, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    119
    Registration Numbers
    119
    Same Product Code
    127
    Applicant Total
    2
    Review Days
    116

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    Basic Information

    Device Name
    Accuryn Monitoring System
    K Number
    K153655
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5130
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Unknown
    Statement or Summary
    Summary
    Applicant
    Potrero Medical, Inc.
    Date Received
    December 21, 2015
    Decision Date
    April 15, 2016
    Product Code
    EZL
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    EZL Catheter, Retention Type, Balloon

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    Other Clearances by Potrero Medical, Inc.

    K Number Device Name
    K221020 Accuryn Monitoring System, Accuryn SmartFoley IAP UO Temp Tray System 12 F, Accuryn SmartFoley IAP UO Temp Tray System 14 F