[Congressional Bills 116th Congress]
[From the U.S. Government Publishing Office]
[H.R. 6261 Introduced in House (IH)]
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116th CONGRESS
2d Session
H. R. 6261
To provide for coverage of testing for COVID-19 at no cost sharing for
Indians receiving health services through the Indian Health Service,
and for other purposes.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
March 12, 2020
Mr. Ruiz introduced the following bill; which was referred to the
Committee on Natural Resources, and in addition to the Committee on
Energy and Commerce, for a period to be subsequently determined by the
Speaker, in each case for consideration of such provisions as fall
within the jurisdiction of the committee concerned
_______________________________________________________________________
A BILL
To provide for coverage of testing for COVID-19 at no cost sharing for
Indians receiving health services through the Indian Health Service,
and for other purposes.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. COVERAGE OF TESTING FOR COVID-19 AT NO COST SHARING FOR
INDIANS RECEIVING HEALTH SERVICES THROUGH INDIAN HEALTH
SERVICE.
The Secretary of Health and Human Services shall cover, without the
imposition of any cost sharing requirements, the cost of providing the
following items and services furnished during any portion of the
emergency period defined in paragraph (1)(B) of section 1135(g) of the
Social Security Act (42 U.S.C. 1320b-5(g)) beginning on or after the
date of the enactment of this Act to Indians (as defined in section 4
of the Indian Health Care Improvement Act (25 U.S.C. 1603)) receiving
health services through the Indian Health Service, regardless of
whether such items or services have been authorized under the contract
health services system funded by the Indian Health Service or are
covered as a health service of the Indian Health Service:
(1) In vitro diagnostic products (as defined in section
809.3(a) of title 21, Code of Federal Regulations) for the
detection of SARS-CoV-2 or the diagnosis of the virus that
causes COVID-19 that are approved, cleared, or authorized under
section 510(k), 513, 515, or 564 of the Federal Food, Drug, and
Cosmetic Act, and the administration of such in vitro
diagnostic products.
(2) Health care provider office visits, urgent care center
visits, and emergency room visits relating to testing for
COVID-19.
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