Who Needs a Lawyer in the Eleventh Circuit?
Drug & Device Law
AUGUST 22, 2022
The plaintiff in Jacob sued the manufacturer of a Class III, FDA premarket-approved medical device. First, the plaintiff’s non-parallel claims were “preempted to the extent” that they would have imposed “alleged labeling or manufacturing requirements that are different from, or in addition to, those imposed by the FDA.” 341 (2001).
59 
Let's personalize your content