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

    RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A

    K Number: K111748 · Decision Nov 23, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    129
    Registration Numbers
    129
    Same Product Code
    349
    Applicant Total
    1
    Review Days
    154

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    Basic Information

    Device Name
    RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A
    K Number
    K111748
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.5800
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Joy Long
    Date Received
    June 22, 2011
    Decision Date
    November 23, 2011
    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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