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As noted above, FDAfollowing its established approach to non-tobacco nicotine productsinitially argued that ENDS that contain tobacco-derived nicotine were drug delivery devices

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MD-Unet performed the best across all evaluation metrics for lesion segmentation, with CPA, Recall, IoU, F1 and Dice scores of 92.75%, 90.94%, 84.93%, 91.81% and 94.67%, respectively