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

    MODEL 20 DIGITAL PULSE RATE MONITOR

    K Number: K780937 · Decision Aug 31, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    103
    Registration Numbers
    103
    Same Product Code
    338
    Applicant Total
    1
    Review Days
    84

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    Basic Information

    Device Name
    MODEL 20 DIGITAL PULSE RATE MONITOR
    K Number
    K780937
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2300
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Sentronix, Inc.
    Date Received
    June 8, 1978
    Decision Date
    August 31, 1978
    Product Code
    DRT
    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
    DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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