Test used must be approved by United States Food and Drug Administration; requirements for administration of test.
Nev. Rev. Stat. § 442.630
in effect1. 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.
Source: NV Statutes (Official Site)URL: https://www.leg.state.nv.us/nrs/NRS-442.htmlFetched: 10/4/2026