FDA Meeting to discuss External Defibrillators

On December 15th and 16th, the FDA held a public discussion/presentation forum on External Defibrillators.  Though I was unable to attend (I was registered, but was called to classes on those days), I have spent the last several days going through the Webcast that was broadcast.  You can find the session at www.fda.gov.

I am, in many ways, glad that I was not able to attend.  I have many strong opinions based upon the presentations and public comments and would have likely spoken in a manner that may not have been perceived as kind.  I found myself yelling Bullshit at my computer screen several times during the presentation.

Instead, I will use my own forum to voice my own opinions and concerns. 

Stay tuned over this weekend for several postings on topics such as:

  • EMT Training in AEDs
  • Public Training in AEDs
  • Which AED manufacturers actually presented vs. which stayed silent. (What does that say for culpability?)
  • Outsourcing of manufacturing and the impact on AED safety and reliability.
  • Manufacturer responsibility for outsourced products.
  • Standardization vs. non-Standardization of AED design and function.
  • Who is responsible for an AED not being “Rescue-Ready?”  The manufacturer or the client?

About sescpr

This is the Official Blog of Safety Education Specialists. An Authorized American Heart Association Training Site located in Virginia, USA. www.ses911.com for all our course listings and information.
This entry was posted in 2010 Guidelines, AED, AED Safety, CPR Class, CPR in the Real World, eLearning, Hands-Only. Bookmark the permalink.

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