Decision Diagnostics Corp (DECN)

[Jelly Bean]

I visited this site and found the original FDA decision summary that listed this:

Special instrument requirements:
LifeScan OneTouch Ultra, Ultra2 and UltraMini blood glucose meters purchased before July 2010 and GenStrip test strips with calibration codes 4, 10, and 13.

I have long wondered about this designation and have heard anecdotal evidence that this restriction was lifted. There is also a subsequent study don't by Pharmetec that indicates the subsequent meters and test strip combo's work fine but there is no FDA follow up report or summary....why?