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

    CRIT-SCAN

    K Number: K910077 · Decision Jun 2, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    400
    Registration Numbers
    400
    Same Product Code
    725
    Applicant Total
    2
    Review Days
    510

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    Basic Information

    Device Name
    CRIT-SCAN
    K Number
    K910077
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2700
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Noninvasive Medical Technology Corp.
    Date Received
    January 9, 1991
    Decision Date
    June 2, 1992
    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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    Other Clearances by Noninvasive Medical Technology Corp.

    K Number Device Name
    K924167 CRIT-LINE