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    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

    BMC CATHETER CONNECTOR CABLE, MODEL RFP-101

    K Number: K023334 · Decision Dec 31, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    139
    Registration Numbers
    139
    Same Product Code
    104
    Applicant Total
    28
    Review Days
    85

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    Basic Information

    Device Name
    BMC CATHETER CONNECTOR CABLE, MODEL RFP-101
    K Number
    K023334
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2900
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Baylis Medical Co., Inc.
    Date Received
    October 7, 2002
    Decision Date
    December 31, 2002
    Product Code
    DSA
    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
    DSA Cable, Transducer And Electrode, Patient, (Including Connector)

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