The US Food and Drug Administration wants to give the machine used for electroconvulsive therapy (ECT or electroshock) a rubber stamp of approval without ever having investigated the device for safety or effectiveness. It takes just a moment to say “no” to this reclassification, and time is running out!
Your Deadline: Friday, 8 January 2010!
It takes just a moment to comment via the FDA web site here:
At least say:
“I oppose the FDA’s proposed reclassification of the ECT device to Class II. The FDA should investigate the ECT device for safety. The FDA should call for Pre-Market Approval Applications for the device.”
Electroshock devices run electricity through the head, typically givento older women diagnosed with clinical depression. For decades, the USFDA never got around to investigating the device for safety andefficacy. Rather than do its job, the FDA is now proposing toreclassify the device. The FDA will accept your public comment untilFriday, 8 January 2010.