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IMGGorBust

05/26/10 11:52 AM

#17183 RE: recon #17182

Great post, Recon. I was thinking of responding myself, but it falls on deaf ears with him, so I didn't bother, but I'm glad you did.

I would also add that Dean had already collected hundreds of signed written Letters of Intent to buy from hospitals and clinics all over the country until the FDA asked the Company to stop accepting them. Since then, they have received hundreds more (perhaps thousands) of verbal commitments to buy upon approval.

I would so there is no doubt about the value of this product. We just need the FDA to get it done within the 60 days it has set for itself as a goal, and which it meets 90% of the time.
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mr_sano

05/26/10 11:57 AM

#17185 RE: recon #17182

Dean has never received a 510K for a complete device like DVIS only mods to existing equipment. Let compare apples to apples shall we?. This likely explain the reason why we are 3+ years after submittal with no approval.

Wants to looks unprofitable to IRS...???LOL!!!!!He doing a great job at that one I'll give you that!

F&S again are you guys serious? do you DD on F&S and you will get your answer. I would bet that if your look at IMGG records you will see that they have employed F&S for consultation service during that time period. Lets ask them.