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Re: Dr. Mugs post# 21418

Thursday, 07/29/2010 2:28:24 PM

Thursday, July 29, 2010 2:28:24 PM

Post# of 59551
Great question mugs... As far as what I've gathered, this is my understanding. The FDA is reviewing not only the structure and design (hardware mechanics) of the DViS, but more importantly the data, output, and results of the experience the patient will potentially undergo using this medical device. They want to make sure the radiation levels are safe, whether the machine is set to 2/10th's of a second or up to 8/10th's of a second, etc... Dean's obligation is to show the clearest and best images he can possibly deliver to the FDA. Besides a whole packet of numerical data, he also sent them various types of images that the Dominion can process (import/export). Being that this device is a medical IMAGING device, this is obviously necessary. They didn't have any problems with the equivalent predecessor devices' images, however, they had a problem with SOME of the DViS's images. The "The %SYSTEMROOT%\System32\getaddrsbproc86.dll file is missing or damaged." error along with some others arose. For you computer guys, this dynamic-link library file is unique to the average computer and operating system. This is because the Dominion's software installs the proper support files in order to properly display the images constructed in a software image-viewing applet uniquely implemented by Imaging3. The DViS's exported image format contains the best quality resolution and picture display it has to offer. And this is what Dean tried showing them. I believe that he has corrected this issue with them and now they are able to open these and view them as the medical professionals would in the real world.

I don't think the clock has restarted at all because there wasn't a formal letter or 8-k filed. And I don't think we'll be waiting much longer (I know this statement is controversial because of the "3 year long wait"). But I guess time will tell.

And I'm pretty sure that Dean sent the previous FDA team's questions, responses, and answers just to clear up any issues from the past. This process has been a hundred times more miserable to Dean than any of the rest of us.

But nobody can argue with me that as soon as the FDA approves this device, and with all of the people waiting on the sideline mainly because of the bashing that created uncertainty, this stock will explode like a dynamite and bring back all of the people who were once shareholders of IMGG and more. IMO, the worst thing you can do is be one of those people because institutional buyers will hop in with millions of shares before any minions like us can grab ahold of anything.

Time will tell...

GLTU!