Nevada Statutes

§ 442.630 — Test used must be approved by United States Food and Drug Administration; requirements for administration of test

Nevada § 442.630
JurisdictionNevada
Title 40PUBLIC HEALTH AND SAFETY
Ch. 442Maternal
TESTING OF PREGNANT WOMEN AND NEWBORN CHILDREN FOR HUMAN IMMUNODEFICIENCY VIRUS

This text of Nevada § 442.630 (Test used must be approved by United States Food and Drug Administration; requirements for administration of test) is published on Counsel Stack Legal Research, covering Nevada primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Nev. Rev. Stat. § 442.630 (2026).

Text

1. Any test for the human immunodeficiency virus, including, without limitation, a rapid test, that is used to carry out the provisions of NRS 442.600 to 442.660 , inclusive, must be approved by the United States Food and Drug Administration. 2. Each test administered to a woman or performed on a child pursuant to the provisions of NRS 442.600 to 442.660 , inclusive, must be administered or performed in accordance with:

(a)The provisions of chapter 652 of NRS and any regulations adopted pursuant thereto; and
(b)The Clinical Laboratory Improvement Amendments of 1988, Public Law No. 100-578, 42 U.S.C. § 263a, if applicable.

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Related

§ 263a
42 U.S.C. § 263a

Legislative History

(Added to NRS by 2007, 2367 )

Nearby Sections

15
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Bluebook (online)
Nevada § 442.630, Counsel Stack Legal Research, https://law.counselstack.com/statute/nv/442.630.