Federal Register: FDA Reclassifies IntuiTap Medical Spinal Imaging System to Expand Access to Neuraxial Procedure Tech
October 31, 2026
October 31, 2026
WASHINGTON, Oct. 31 (TNSFR) -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following action in the Federal Register.
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Medical Devices; Anesthesiology Devices; Classification of the Spinal Imaging System for Neuraxial Procedures
The Food and Drug Administration (FDA) is classifying the spinal imaging system for neuraxial procedures into class II. The special controls that apply to the device type are identifi . . .
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Medical Devices; Anesthesiology Devices; Classification of the Spinal Imaging System for Neuraxial Procedures
The Food and Drug Administration (FDA) is classifying the spinal imaging system for neuraxial procedures into class II. The special controls that apply to the device type are identifi . . .