§ 442.630 — Test used must be approved by United States Food and Drug Administration; requirements for administration of test
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.
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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:
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Nevada § 442.630, Counsel Stack Legal Research, https://law.counselstack.com/statute/nv/442.630.