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

    CAMINO COMPARTMENTAL PRESS MONITOR CATH/110-4D

    K Number: K863969 · Decision May 27, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    64
    Registration Numbers
    64
    Same Product Code
    63
    Applicant Total
    18
    Review Days
    225

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    Basic Information

    Device Name
    CAMINO COMPARTMENTAL PRESS MONITOR CATH/110-4D
    K Number
    K863969
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2870
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Camino Laboratories, Inc.
    Date Received
    October 14, 1986
    Decision Date
    May 27, 1987
    Product Code
    DXO
    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
    DXO Transducer, Pressure, Catheter Tip

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