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

    A-V(TM) SOFTOUCH UHF CARDIAC PIGTAIL

    K Number: K885348 · Decision May 15, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    210
    Registration Numbers
    211
    Same Product Code
    499
    Applicant Total
    7
    Review Days
    138

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    Basic Information

    Device Name
    A-V(TM) SOFTOUCH UHF CARDIAC PIGTAIL
    K Number
    K885348
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1200
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Mallinckroot, Inc.
    Date Received
    December 28, 1988
    Decision Date
    May 15, 1989
    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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