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

    PULSTAR LOGIX INTERMITTENT PNEUMATIC COMPRESSION SYSTEM

    K Number: K123308 · Decision Feb 8, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    129
    Registration Numbers
    129
    Same Product Code
    349
    Applicant Total
    2
    Review Days
    107

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    Basic Information

    Device Name
    PULSTAR LOGIX INTERMITTENT PNEUMATIC COMPRESSION SYSTEM
    K Number
    K123308
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.5800
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Albahealth, LLC
    Date Received
    October 24, 2012
    Decision Date
    February 8, 2013
    Product Code
    JOW
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JOW Sleeve, Limb, Compressible

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    Other Clearances by Albahealth, LLC

    K Number Device Name
    K141609 PULSTAR LOGIX PUMP