US lawFederal (United States)Session lawPub. L. 110-85 — To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and for medical devices, to enhance the postmarket authorities of the Food and Drug Administration with respect to the safety of drugs, and for other purposes.301Pub. L. 110-85, tit. III, sec. 301SHORT TITLE.EnactedYear: 2007Length: 20 wordsOfficial source SEC. 301. SHORT TITLE. This title may be cited as the “Pediatric Medical Device Safety and Improvement Act of 2007”.PreviousPub. L. 110-85, tit. II, sec. 201NextPub. L. 110-85, tit. III, sec. 302