In Westlaw Today, Attorneys Examine Three FDA Draft Guidances to Modernize Medical Device

In The News
September 29, 2023

In a Westlaw Today article, FDA partners Greg Levine and Joshua Oyster and FDA associate Michael Purcell discussed three draft guidance documents the Food and Drug Administration issued to modernize the medical device marketing authorization pathway under Section 510(k) of the Food, Drug and Cosmetic Act.