Federal Register: FDA Reclassifies Whole Room Microbial Reduction Devices to Ease Healthcare Disinfection Access
September 11, 2026
September 11, 2026
WASHINGTON, Sept. 11 (TNSFR) -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following action in the Federal Register.
* * *
Medical Devices; General Hospital and Personal Use Devices; Classification of the Whole Room Microbial Reduction Device
The Food and Drug Administration (FDA) is classifying the whole room microbial reduction device into class II. The special controls that apply to the device type are identi . . .
* * *
Medical Devices; General Hospital and Personal Use Devices; Classification of the Whole Room Microbial Reduction Device
The Food and Drug Administration (FDA) is classifying the whole room microbial reduction device into class II. The special controls that apply to the device type are identi . . .