BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

    BM-103 BATTERY MODULE

    K Number: K883877 · Decision Oct 28, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    400
    Registration Numbers
    400
    Same Product Code
    725
    Applicant Total
    55
    Review Days
    45

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    Basic Information

    Device Name
    BM-103 BATTERY MODULE
    K Number
    K883877
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2700
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Datex Division Instrumentarium Corp.
    Date Received
    September 13, 1988
    Decision Date
    October 28, 1988
    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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