2011 Nevada Revised Statutes
Chapter 442 - Maternal and Child Health; Abortion
NRS 442.630 - Test used must be approved by United States Food and Drug Administration; requirements for administration of test.
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.
(Added to NRS by 2007, 2367)
Disclaimer: These codes may not be the most recent version. Nevada may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
