21 CFR § 808.73
Minnesota
June 25, 2020
The following Minnesota medical device requirements are preempted by section 521(a) of the act, and the Food and Drug Administration has denied them an exemption from preemption under section 521(b) of the act: Minnesota Statutes, sections 145.43 and 145.44.
[45 FR 67336, Oct. 10, 1980]
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