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

    MICOR CONDUCTION CATHETER

    K Number: K001717 · Decision Sep 20, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    55
    Registration Numbers
    55
    Same Product Code
    74
    Applicant Total
    8
    Review Days
    107

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    Basic Information

    Device Name
    MICOR CONDUCTION CATHETER
    K Number
    K001717
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5120
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Micor, Inc.
    Date Received
    June 5, 2000
    Decision Date
    September 20, 2000
    Product Code
    BSO
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    BSO Catheter, Conduction, Anesthetic

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    Other Clearances by Micor, Inc.

    K Number Device Name
    K031600 CONDUCTION CATHETER
    K003966 WUNDCATH CONDUCTION CATHETER
    K001940 MICOR ANESTHESIA CONDUCTION KIT
    K991879 SPRING-WOUND EPIDURAL CATHETER
    K861008 PERCUTANEOUS CATHETERS
    K860339 PERCUTANEOUS CATHETERS
    K854018 ANGIOGRAPHY CATHETERS