Obamacare Mandatory RFID Chipping Now Being Implemented In Wyoming”?
Yet another fatal blow to American privacy and liberties.
In Hanna, Wyoming, the Obamacare RFID chips are currently being “test ran.”
Over the last two weeks there has been legislation that has passed that mandates anyone who is receiving government welfare or any sort of government assistance, to get the RFID implant. It doesn’t stop with welfare recipients though. This fascist invasion extends to all Police officers, military and even garbage men will be required to have the RFID chip by the end of next month or face termination from their jobs.
Full Story Here >>>> http://tinyurl.com/Forcedchip
Q:Is This For Real ? A:Yes This Is Real Please Read all The Facts Below
The Section of the Bill in Question
The following section of the ObamaCare Bill (H.R. 3590) is the root of the ObamaCare microchip rumor. As you can see there is no mandatory chip implant, however it does allow data collection from implanted devices. The main idea of this section of the bill is to collect medical information to better treat patients.
H.R. 3590 amends Section 519 of the Food, Drug and Cosmetic Act (21 U.S.C .360i). Here is the applicable language from H.R. 3590 (page 1,014):(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.
Read More Here >>>http://obamacarefacts.com/obamacare-microchip-implant.php
Class II – Most medical devices are considered Class II devices. Examples of Class II devices include powered wheelchairs and some pregnancy test kits. 43% of medical devices fall under this category.
Guidance for Industry and FDA Staff Class II Special Controls Guidance Document: Implantable Radiofrequency Transponder System for Patient Identification and Health Information
Document issued on: December 10, 2004 Please Read The Risk To health Section click here to see full document >>> http://tinyurl.com/riskstoyourhealth
Class III devices are defined as those devices for which insufficient information exists to assure their safety and effectiveness solely through general or special controls. They often support or sustain human life, are of substantial importance in preventing impairment of human health, or present a potential, unreasonable risk of illness or injury. Class III devices require Premarket Approval (PMA) before they can be legally marketed. This process of scientific review is required in order to provide reasonable assurance of safety and effectiveness of Class III devices. PMA approval is based on a determination by FDA that the PMA submission contains sufficient valid scientific evidence to provide reasonable assurance that the device is safe and effective for its intended use(s). Post-approval studies may be required as a condition of PMA approval in order to provide additional long-term data. Read Full Document Here >>> http://tinyurl.com/classIII
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