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Technologies · 30/10/20261 min de lecture
Medical Devices; General and Plastic Surgery Devices; Classification of the Software-Aided Adjunctive Diagnostic Device for Use by Physicians on Lesions Suspicious for Skin Cancer
Traduction automatique locale · Langue originale de la source
Résumé
The Food and Drug Administration (FDA) is classifying the software-aided adjunctive diagnostic device for use by physicians on lesions suspicious for skin cancer into class II (special controls).
Langue originale de la source: Federal Register — Health and Human ServicesOuvrir le communiqué original →