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52 FR 16122, May 1, 1987, unless otherwise noted.
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Nomenclature changes to part 862 appear at 73 FR 35341, June 23, 2008.
(a) Identification. A propoxyphene test system is a device intended to measure propoxyphene, a pain-relieving drug, in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of propoxyphene use or overdose or in monitoring levels of propoxyphene to ensure appropriate therapy.
(b) Classification. Class II (special controls). A propoxyphene test system is not exempt if it is intended for any use other than employment or insurance testing. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 862.9, provided the test system is intended for employment and insurance testing and includes a statement in the labeling that the device is intended solely for use in employment and insurance testing.
[52 FR 16122, May 1, 1987, as amended at 84 FR 71798, Dec. 30, 2019; 91 FR 63487, Oct. 6, 2026]