21 CFR § 808.67
Kentucky
June 25, 2020
The following Kentucky medical device requirement is preempted by section 521(a) of the act, and the Food and Drug Administration has denied it an exemption from preemption under section 521(b) of the act: Kentucky Revised Statutes, section 334.200(1).
[45 FR 67336, Oct. 10, 1980]
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