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Alias Born 11/18/2011

Re: None

Saturday, 11/19/2011 12:39:58 PM

Saturday, November 19, 2011 12:39:58 PM

Post# of 330169
Here is why BIEL devices will never be approved for FDA clearance in Class 2 or Class 1, ever: The lack of substantial evidence, flawed studies and potential danger. Pregnant women, people with pace makers etc. Allay and Actipatch cannot be approved OTC, period. Prescription may be done, but docs will gravitate toward larger dollar devices, rather than $30 solutions. It's economics. Recovery RX will not be accepted by professional physicians as there are far more proven and effective and billable alternatives. Too many questions of efficacy and safety from FDA. It will be years if ever, PEMF technology is approved OTC by FDA. Not going to happen people. BIEL is doing its best to kick the can down the road with hopeful PRs etc. Cash it in and move on.