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21 CFR 868.2025

§ 868.2025 Ultrasonic air embolism monitor.

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 868.2025, § 868.2025 Ultrasonic air embolism monitor, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/89745
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(a) Identification. An ultrasonic air embolism monitor is a device used to detect air bubbles in a patient's blood stream. It may use Doppler or other ultrasonic principles. (b) Classification. Class II (performance standards).

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.