BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    MICROCAP PLUS/NPB-75

    K Number: K024300 · Decision Apr 3, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    400
    Registration Numbers
    400
    Same Product Code
    725
    Applicant Total
    19
    Review Days
    100

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    Basic Information

    Device Name
    MICROCAP PLUS/NPB-75
    K Number
    K024300
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.2700
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Oridion Medical 1987 , Ltd.
    Date Received
    December 24, 2002
    Decision Date
    April 3, 2003
    Product Code
    DQA
    Advisory Committee
    Cardiovascular
    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
    DQA Oximeter

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