Skadden: FDA's Center for Devices and Radiological Health Releases Two Preliminary Reports with Recommendations for the 510(k) Premarket Notification Process | Practical Law

Skadden: FDA's Center for Devices and Radiological Health Releases Two Preliminary Reports with Recommendations for the 510(k) Premarket Notification Process | Practical Law

This Skadden, Arps, Slate, Meagher & Flom LLP memorandum discusses two preliminary reports released by the Center for Devices and Radiological Health of the Food and Drug Administration (FDA) making recommendations addressing the FDA's regulation of medical devices. 

Skadden: FDA's Center for Devices and Radiological Health Releases Two Preliminary Reports with Recommendations for the 510(k) Premarket Notification Process

by Skadden, Arps, Slate, Meagher & Flom LLP
Published on 13 Aug 2010 • USA (National/Federal)
This Skadden, Arps, Slate, Meagher & Flom LLP memorandum discusses two preliminary reports released by the Center for Devices and Radiological Health of the Food and Drug Administration (FDA) making recommendations addressing the FDA's regulation of medical devices.