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21 CFR 882.1935

§ 882.1935 Near Infrared (NIR) Brain Hematoma Detector.

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

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21 CFR 882.1935, § 882.1935 Near Infrared (NIR) Brain Hematoma Detector, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/90673
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(a) Identification. A Near Infrared (NIR) Brain Hematoma Detector is a noninvasive device that employs near-infrared spectroscopy that is intended to be used to evaluate suspected brain hematomas. (b) Classification. Class II (special controls). The special controls for this device are: (1) The sale, distribution, and use of this device are restricted to prescription use in accordance with § 801.109 of this chapter; (2) The labeling must include specific instructions and the clinical training needed for the safe use of this device; (3) Appropriate analysis/testing should validate electromagnetic compatibility (EMC), electrical safety, and battery characteristics; (4) Performance data should validate accuracy and precision and safety features; (5) Any elements of the device that may contact the patient should be demonstrated to be biocompatible; and, (6) Appropriate software verification, validation, and hazard analysis should be performed.

Legislative history

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