Бізнес · 16.05.20131 хв читання
Medical Devices; General Hospital and Personal Use Monitoring Devices; Classification of the Ingestible Event Marker
Локальний автоматичний переклад · Оригінальна мова джерела
Короткий зміст
The Food and Drug Administration (FDA) is classifying the ingestible event marker into class II (special controls). The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.