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Updated: Feb 3, 2026

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Thermal Measurement Techniques in Analytical Microfluidic Devices
Published on: June 3, 2015
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Medical Devices; General and Plastic Surgery Devices; Classification of the Wound Autofluorescence Imaging Device.
Federal Register
|October 26, 2018
Abstract:
The Food and Drug Administration (FDA or we) is classifying the wound autofluorescence imaging device into class I. We are taking this action because we have determined that classifying the device into class I will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
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