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

    NORMOCAP CR-102, RECORDER UNIT

    K Number: K802762 · Decision Nov 26, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    82
    Registration Numbers
    82
    Same Product Code
    120
    Applicant Total
    2
    Review Days
    22

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    Basic Information

    Device Name
    NORMOCAP CR-102, RECORDER UNIT
    K Number
    K802762
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.1720
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Instrumentarium-Datex
    Date Received
    November 4, 1980
    Decision Date
    November 26, 1980
    Product Code
    CCL
    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
    CCL Analyzer, Gas, Oxygen, Gaseous-Phase

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    Other Clearances by Instrumentarium-Datex

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