eCFR Reference Browser

---

title: "21 CFR §808.59"

source: "https://www.ecfr.gov/current/title-21/section-808.59"

title_number: "21"

volume_number: "8"

chapter_number: "Unknown"

subchapter_code: "H"

subchapter_subject: "MEDICAL DEVICES"

part_code: "808"

part_subject: "EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS"

subpart_code: "C"

subpart_subject: "Listing of Specific State and Local Exemptions"

section_number: "808.59"

section_subject: "Florida."

cfr_reference: "21 CFR 808.59"

title_name: "Title 21"

title_subject: "Food and Drugs"

parts_covered: "Parts 800 to 1299"

revised_date: "Revised as of April 1, 2019"

publication_date: "As of April 1, 2019"

contains_description: "Containing a codification of documents of general applicability and future effect"

publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"

---

The following Florida 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:

(a)Florida Statutes, section 468.135(5).

(b)Florida Administrative Code, section 10D-48.25(26).

§808.59 - Florida.