H. R. 2372 aims to amend the Federal Food, Drug, and Cosmetic Act to improve the reporting and communication of medical device information, focusing on design changes and reprocessing instructions. It requires manufacturers to notify the Secretary before making device design...
Simple Explanation
The bill, H.R. 2372, is like a set of new rules to make sure people who make medical devices tell others about important changes and how to clean them properly so they don't make anyone sick.