That year, a new law for the first time classified medical devices into three risk categories, with clinical data required only for devices in the highest-risk category, Class III. The FDA has yet ...
Shares of ResMed and Inspire Medical Systems fell after the FDA approved Eli Lilly's weight ... doctors will prescribe using both drugs and devices such as his company makes together to help ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback