2003P-0555 - Maintain the Electroconvulsive Therapy Device in Class III for All Indications
FDA Comment Number : EC25
Submitter : Mrs. Gloria Becker Date & Time: 06/10/2004 05:06:43
Organization : Rehabilitation Services
Individual Consumer
Category :
Issue Areas/Comments
GENERAL
GENERAL
I support the FDA maintaining the ECT device in Class III, where the risks outweigh benefits.