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

    MODEL 303D AND 403D ADULT HEART RATE & RESPIRATOR

    K Number: K880066 · Decision Mar 22, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    103
    Registration Numbers
    103
    Same Product Code
    338
    Applicant Total
    27
    Review Days
    71

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    Basic Information

    Device Name
    MODEL 303D AND 403D ADULT HEART RATE & RESPIRATOR
    K Number
    K880066
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2300
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Ivy Biomedical Systems, Inc.
    Date Received
    January 11, 1988
    Decision Date
    March 22, 1988
    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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