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

    EMBOCATH PLUS INFUSION MICROCATHETER, MODEL ECP-100 AND ECP-135

    K Number: K062126 · Decision Aug 9, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    210
    Registration Numbers
    211
    Same Product Code
    499
    Applicant Total
    6
    Review Days
    14

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    Basic Information

    Device Name
    EMBOCATH PLUS INFUSION MICROCATHETER, MODEL ECP-100 AND ECP-135
    K Number
    K062126
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1200
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Biosphere Medical, Inc.
    Date Received
    July 26, 2006
    Decision Date
    August 9, 2006
    Product Code
    DQO
    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
    DQO Catheter, Intravascular, Diagnostic

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