Part 882 Subpart B—Neurological Diagnostic Devices

FDA submissions for Part 882 Subpart B—Neurological Diagnostic Devices in the Ophthalmic (OP) review panel, including product codes and regulations.

Section range: § 882.1935

CFR Part: 882

Product Codes

Product Code	Device Name	Regulation	Class	Devices
OPT	Infrared Hematoma Detector	882.1935	2	5

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