Zdrowie i gospodarka · 24/08/1995

FDA Mandates Premarket Approval for Cranial Electrotherapy Stimulators

The FDA is requiring manufacturers to submit premarket approval applications or product development protocols for cranial electrotherapy stimulators, a medical device, in order to continue commercial distribution, with a 90-day deadline

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

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