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Subject Everyone to receive a chip implant via the Health Care Bill
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Original Message Page 1001-1008 of the H.R. 3200, “America’s Affordable Health Choices Act”

Explains that they will implement a national medical device that will be implantable (AKA the chip or if you are a bible reader "the mark of the beast".

This in and of its self should get some fighting mad. Will it you? This ACT is against all that a true American stands for. (Get up stand up, stand up for your rights) Read it for your selves!

I of course para-phrased this section but it would do you well to read it yourself.

[link to waysandmeans.house.gov]

Subtitle C—National Medical
10 Device Registry
11 SEC. 2521. NATIONAL MEDICAL DEVICE REGISTRY.

‘‘National Medical Device Registry
21 ‘‘(g)(1) The Secretary shall establish a national med
22 ical device registry (in this subsection referred to as the
23 ‘registry’) to facilitate analysis of postmarket safety and
24 outcomes data on each device that—
25 ‘‘(A) is or has been used in or on a patient; and
‘‘(B) is—
2 ‘‘(i) a class III device; or
3 ‘‘(ii) a class II device that is implantable,

(under Cornell law school:
[link to assembler.law.cornell.edu]

A class III device and a class II device means: (i) shall be submitted in accordance with part 803 of title 21, Code of Federal Regulations (or successor regulations), unless the Secretary grants an exemption or variance from, or an alternative to, a requirement under such regulations pursuant to section 803.19 of such part, if the device involved is—
(I) a class III device;
(II) a class II device that is permanently implantable, is life supporting, or is life sustaining; or
(III) a type of device which the Secretary has, by notice published in the Federal Register or letter to the person who is the manufacturer or importer of the device, indicated should be subject to such part 803 in order to protect the public health; )

‘‘(iii) other postmarket device surveillance
10 activities of the Secretary authorized by this
11 chapter; and

‘‘(4) Not later than 36 months after the date of the
22 enactment of this subsection, the Secretary shall promul23
gate regulations for establishment and operation of the
24 registry under paragraph (
1). Such regulations—

‘‘(5) To carry out this subsection, there are author13
ized to be appropriated such sums as may be necessary
14 for fiscal years 2010 and 2011
.’’.
15 (2) EFFECTIVE DATE.—The Secretary of
16 Health and Human Services shall establish and
17 begin implementation of the registry under section
18 519(g) of the Federal Food, Drug, and Cosmetic
19 Act, as added by paragraph (1), by not later than
20 the date that is 36 months after the date of the en
21 actment of this Act, without regard to whether or
22 not final regulations to establish and operate the
23 registry have been promulgated by such date.
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