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

    SIRECUST MODEL 960 AND 961 PATIENT MONITORING

    K Number: K872249 · Decision Jul 21, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    103
    Registration Numbers
    103
    Same Product Code
    338
    Applicant Total
    2
    Review Days
    39

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    Basic Information

    Device Name
    SIRECUST MODEL 960 AND 961 PATIENT MONITORING
    K Number
    K872249
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2300
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Medical Electronics Laboratories, Inc.
    Date Received
    June 12, 1987
    Decision Date
    July 21, 1987
    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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    Other Clearances by Medical Electronics Laboratories, Inc.

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    K873533 SIEMENS SIRECUST 1280, 1281 W/ARRHYTHMIA SOFTWARE