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

    BLOOD PRESSURE MODULE

    K Number: K780571 · Decision May 9, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    36
    Registration Numbers
    36
    Same Product Code
    26
    Applicant Total
    5
    Review Days
    29

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    Basic Information

    Device Name
    BLOOD PRESSURE MODULE
    K Number
    K780571
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2060
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    C-V Monitors Corp.
    Date Received
    April 10, 1978
    Decision Date
    May 9, 1978
    Product Code
    DRQ
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DRQ Amplifier And Signal Conditioner, Transducer Signal

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    Other Clearances by C-V Monitors Corp.

    K Number Device Name
    K792099 50MM WRITER MODEL CVM 9529
    K790004 MONITOR SCOPES, MODELS 9502, 9503
    K781867 WRITER, GEMINI-3
    K780572 DCG PREAMPLIFIER MODULE