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

    MONITOR, PATIENT (MODEL 78333A)

    K Number: K760160 · Decision Jul 19, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    101
    Registration Numbers
    101
    Same Product Code
    334
    Applicant Total
    230
    Review Days
    17

    Basic Information

    Device Name
    MONITOR, PATIENT (MODEL 78333A)
    K Number
    K760160
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2300
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    HEWLETT-PACKARD CO.
    Date Received
    July 2, 1976
    Decision Date
    July 19, 1976
    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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