ECT Device Safety: Attorney Barry Kade to the FDA, 2009
Attorney Barry Kade to the FDA, ECT device reclassification, 2009.
0 Comments
June 17, 2022
ECT Device Safety – New York Association of Psychiatric Rehabilitation Services (NYAPRS) to the FDA, 2010
ECT Device Safety - New York Association of Psychiatric Rehabilitation Services (NYAPRS) to the FDA, 2010
May 24, 2022
ECT Device Safety : Center for the Human Rights of Users and Survivors of Psychiatry to the FDA
Center for the Human Rights of Users and Survivors of Psychiatry to the FDA, 2009
May 23, 2022
ECT Safety Reclassification: Psych Rights to FDA
Psych Rights to FDA on the 2016 ECT device safety reclassification.
May 20, 2022
ECT Safety Reclassification: Psychiatrist Daniel P. Fisher to FDA, 2011
Psychiatrist Daniel P. Fisher to the FDA on the ECT device reclassifications, 2011.
May 12, 2022
ECT Safety Reclassifcation – Mental Hygiene Legal Service to FDA, 2009
We are attorneys with a public agency concerned with mental health issues in New York State, and in that context write this letter in opposition to the above-docketed proposal to reclassify from Class Ill to Class Il devices used to administer electro-convulsive therapy ("ECT", also commonly referred to as electro-shock or shock treatment).
January 6, 2022