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Re: None

Friday, 05/03/2019 3:42:15 PM

Friday, May 03, 2019 3:42:15 PM

Post# of 329294
Well, next Friday is the 90 day deadline, per the recent 510(k) submission by BIEL. If the clearance doesn't come through by then, IMO, it's not going to happen. Ya know, this just might be last last hurrah for BIEL, IMO. My premise is based on the following reasons. First of all, the CEO apparently, only believes a successful "acid test" from the FDA is the only thing worthy of a PR. Furthermore, he has a dogged aversion toward advertising. Thus, asking for failure! He has two FDA approved Actipatch derivations in his back pocket for two years now, if I'm not mistaken, and what did that get us? Presently, having front-runner status, in regards to the technology, IMO, could be lost sooner than one might think. For, the image in the rear view mirror of the competition is closer than you think". We have a winner in Actipatch, IMO, but the game is being thrown. Maddening!!

GLTA!!!

P.S. The Actipatch patent time limit is being frittered away, day by day! Sad!!