BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

    ANGIO-PRESS LITE DVT Compression Device

    K Number: K173012 · Decision May 10, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    129
    Registration Numbers
    129
    Same Product Code
    349
    Applicant Total
    2
    Review Days
    225

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    Basic Information

    Device Name
    ANGIO-PRESS LITE DVT Compression Device
    K Number
    K173012
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.5800
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Pegasus Medical Supply, Inc.
    Date Received
    September 27, 2017
    Decision Date
    May 10, 2018
    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 Pegasus Medical Supply, Inc.

    K Number Device Name
    K143202 ANGIO-PRESS DVT Compression Device Model Name: IPCS