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.