FDA Takes No Action on 510(k) Process After IOM Review

May 31, 2016 | Author: meshlawuitcenter | Category: Types, Research

Embed

Donate

Report this link

Description

The Food and Drug Administration (FDA) in 2009 initiated a review of its controversial 510(k) premarket notification pro...

Comments

SUPPORT DOCURI

We need your help!

Thank you for interesting in our services. We are a non-profit group that run this website to share documents. We need your help to maintenance this website.

Donate
Sharing

To keep our site running, we need your help to cover our server cost (about $400/m), a small donation will help us a lot.

No, thanks! Close the box.