FDA and ECT devices

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Uploaded by on Aug 1, 2006

This is the well-known story of how the FDA has been lobbied by the industry to change ECT devices from Class III to Class II. What's interesting (and keeps popping up in Harold's testimony) is that apparently the psych rights movement is having an impact on things. Despite his admitting that he speaks with the FDA regularly, and that the industry has lobbied the FDA for the change, Harold says the FDA is afraid to make a move.

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