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Zorro

07/21/07 8:50 PM

#1132 RE: deanjanes #1131

The FDA is also the lapdog for special interests with politicians as its master and can make or break any innovation or new discovery they want if commanded to do so. GLTY.
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capital gain

07/22/07 10:08 AM

#1133 RE: deanjanes #1131

Dean

Thanks for your reply, lets hope for a quick dicision by the FDA.
I am holding this stock for the long term anyway, as I think your scanner is going to grab a lot a that market in the years to come.
The end of medicine does sound like a very good book, I will bye it in the very near future as well, just need to finish a couple of other books first.

GLTA

A.H
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bluebird50

07/23/07 2:44 PM

#1135 RE: deanjanes #1131

I just stumbled across this stock, very interesting. Is it something you could market in other countries? Not sure if their process is as fickle as ours? Could generate revenue until fda approval. Bluebird
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Raider Nation

04/08/09 7:34 PM

#2729 RE: deanjanes #1131

Dean, in your Post #1131 you had stated "The SEC in our submission required me to inform investors it could take up to 2 years, which is more typical of class III invasive devices requiring extensive clinical studies. Anyway, lets hope for the best and plan for the worst as government agencies defy logic."

Since we submitted the 510(k) to the FDA on June 19, 2007 (http://www.imaging3.com/news_june_19_07.htm <--the news release), am I correct to assume that our "2-year clock" expires on June 19, 2009? If so, then we ought to be looking for some news (and it ought to be soon...)!

Btw, I fully expected this to take the two years that you had already mentioned here. With accumulation going on for so long (see the sideways stock trading action), I can only assume that some others have been expecting this as well; although with a lot of dumping at the 'bid' it seems like we have had our share of non-believers. By the time that the clock strikes the big '2' in June--we will have our answer from the FDA (no pressure, Dean...).