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ECT Device Reclassification : Maryland Disability Law Center to FDA

Maryland Disability Law Center to the FDA on ECT device reclassification, 2009.

ECT Device Reclassification: Disability Rights Montana to FDA

Disability Rights Montana weighs in on the FDA’s proposed ECT device reclassification, 2009.

ECT Device Reclassification : Delaware Developmental Disability Council to FDA, 2009

Delaware Developmental disability council weighs in on FDA’s 2009 proposed safety reclassification to the electroshock device.

Statement to FDA on ECT – Disability Rights Washington

Disability Rights Washington weighs in on FDA’s proposed ECT device safety reclassification, 2009.

Statement for the FDA on Electroconvulsive Therapy (ECT) From the World Institute on Disability

The World Institute on Disability weighs in on 2009 FDA ECT reclassification hearings.

Open Letter to the FDA’s Denial of ECT’s Harms – 2021

I write to appeal your denial of request number: 2020-7319 for the expedited processing of the Electronic Freedom of Information Act request submitted on 9 October 2020. I received your denial October 27, 2020 and have 90 days to appeal your decision.

Appealing the FDA’s Denial of ECT’s Harms

More than 200 people signed an open letter to the FDA requesting electroconvulsive therapy’s safety studies and electrical dosing protocols.

Open Letter of Appeal to FDA about Electroconvulsive Therapy (ECT)

After being injured by ECT, I learned of several risks patients aren’t aware of. I reached out to the FDA to help educate the public. Their response to my FOIA