Sec. 2. (a) The sale or distribution of:
(1) diagnostic testing equipment or apparatus; or
(2) a blood collection kit;
intended for home use to diagnose or confirm human immunodeficiency virus (HIV) infection or disease is prohibited unless the testing equipment, apparatus, or kit has been approved for such use by the federal Food and Drug Administration.
(b) A person who recklessly, knowingly, or intentionally violates this section commits a Class C infraction.
As added by P.L.158-2013, SEC.547. Amended by P.L.174-2021, SEC.79.