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

    ANGIO-PRESS DVT Compression Device Model Name: IPCS

    K Number: K143202 · Decision Jul 7, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    129
    Registration Numbers
    129
    Same Product Code
    349
    Applicant Total
    2
    Review Days
    242

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    Basic Information

    Device Name
    ANGIO-PRESS DVT Compression Device Model Name: IPCS
    K Number
    K143202
    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
    November 7, 2014
    Decision Date
    July 7, 2015
    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
    K173012 ANGIO-PRESS LITE DVT Compression Device