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Zdrowie i gospodarka · 14/01/2020

FDA Grants Exemption for Powered Wheeled Stretchers from Premarket Notification Requirements

The FDA has issued an order exempting powered wheeled stretchers, a Class II medical device, from premarket notification requirements, allowing these devices to be marketed without submitting a 510(k) premarket notification, effective immediately.

Source: Federal Register — Food and Drug AdministrationOpen original release →