The Law goes into effect March 2013 with a NO LATER DATE of Dec 31 2017. So sometime between March 2013 and Dec 2017, it will be mandatory. No one actually knows the exact date. Just look for the Economy to crash soon or a world war.
News Articles:
Want An RFID Chip Implanted Into Your Hand? Here's What The DIY Surgery Looks Like
http://www.forbes.com/sites/andygreen...
Scientists Successfully 'Hack' Brain To Obtain Private Data
http://seattle.cbslocal.com/2012/08/2...
Can snoopers hack your brain?
http://www.foxnews.com/scitech/2012/0...
H.R.4872 Reconciliation Act of 2010 (Reported in House - RH)
http://housedocs.house.gov/rules/hr48...
(You will see ' Section 2521 ' starting on page 1013 - 1014) (NOTICE THIS IS A GOVERNMENT WEBSITE SO IT'S LEGIT)
Wanna know what a Class II device is? FDA put out a document WAY BACK in 2004 (Showing this has been planned even before the Beast Obama got elected).......
http://www.fda.gov/downloads/MedicalD...
Read that 'table of contents' of the document above, right from the FDA themselves. Look at the web address above (FDA.GOV) here is the table of contents.....
A. BIOCOMPATIBILITY
B. INFORMATION SECURITY PROCEDURES (DESIGN AND VALIDATION)
C. SOFTWARE VALIDATION
D. MIGRATION TESTING OF IMPLANTED TRANSPONDER
E. PERFORMANCE TESTING OF IMPLANTED TRANSPONDER
F. PERFORMANCE TESTING OF INSERTER
G. PERFORMANCE TESTING AND HAZARD ANALYSIS OF ELECTRONIC SCANNER
H. ELECTROMAGNETIC COMPATIBILITY
I. ELECTRICAL SAFETY PERFORMANCE TESTING
J. STERILITY
K. MAGNETIC RESONANCE IMAGING COMPATIBILITY
L. LABELING
So you see ladies and gentlemen, this ISN'T the so called 'pacemakers' the Obama camp is telling you it is saying. No, these are 100% RFID Chips under your skin.
Health Care and Education Reconciliation Act of 2010
http://en.wikipedia.org/wiki/Health_C...
OBAMA's Health Care Bill H.R.4872 Reads as Followed in Section 2521 (THIS GOES INTO EFFECT March 2013 with a no later than date of December 2017 ! ! ! )
. (g)(1) The Secretary shall establish a national medical device registry (in this subsection referred to as the `registry') to facilitate analysis of postmarket safety and outcomes data on each device that-- `(A) is or has been used in or on a patient; and `(B) is-- `(i) a class III device; or `(ii) a class II device that is implantable, life-supporting, or life-sustaining.
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