21 C.F.R. · Food and Drugs
21 C.F.R. § 870.5550

External transcutaneous cardiac pacemaker (noninvasive).

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 870.5550 — External transcutaneous cardiac pacemaker (noninvasive).

§ 870.5550 External transcutaneous cardiac pacemaker (noninvasive). (a) Identification. An external transcutaneous cardiac pacemaker (noninvasive) is a device used to supply a periodic electrical pulse intended to pace the heart. The pulse from the device is usually applied to the surface of the chest through electrodes such as defibrillator paddles. (b) Classification. Class II. The special controls for this device are: (1) “American National Standards Institute/American Association for Medical Instrumentation's DF–21 ‘Cardiac Defibrillator Devices’ ” 2d ed., 1996, and (2) “The maximum pulse amplitude should not exceed 200 milliamperes. The maximum pulse duration should not exceed 50 milliseconds.” [45 FR 7907, Feb. 5, 1980, as amended at 52 FR 17737, May 11, 1987; 65 FR 17144, Mar. 31, 2000]

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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21 C.F.R. § 870.5550
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The regulatory text of 21 C.F.R. § 870.5550 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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