Vivos Inc (RDGL)

[Kooka_Duke]

Based On The Reason Why They Where Denied The First Time (In February 2014, the FDA rejected the Company's request for marketing clearance for the same device under Section 510(k) of the Act. The FDA determined that the device was not substantially equivalent, concluding that the device is classified by statute as a Class III medical device, unless the device is reclassified.) ADMD Will Get Clearance To Market The Y-90 RadioGel™ This Time Either Here In The US Or Both The US & Europe.....

The Fact To Remember Is They Have a Product That Save Lives, And The Anticipation Plus The Hype Alone Before We Get Word From The FDA Is Good For a SP In The Pennies!