他向委员会陈述说FDA和联邦贸易委员会具有管理虚假或有误导倾向的医疗器械广告的法定权利。

He told the committee that the FDA and the Federal Trade Commission already have legal authority to regulate false or misleading advertising for medical devices.

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美国食品和药品管理局在非处方药，医疗器械和生物制品领域，向包括消费者和产业界代表在内的咨询委员会进行咨询。

FDA has placed consumer and industry members on advisory committees it consults concerning over-the-counter drugs, medical devices, and biologics.

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这些资金来源依赖于负责开发医疗器械上市后监测系统框架的规划委员会的建议。

The funding is tied to recommendations from the planning board tasked with developing the postmarket medical device surveillance system framework.

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