Skadden: FDA's Center for Devices and Radiological Health Releases Two Preliminary Reports with Recommendations for the 510(k) Premarket Notification Process | Practical Law
Practical Law Article 2-503-2033 (Approx. 2 pages)
Skadden: FDA's Center for Devices and Radiological Health Releases Two Preliminary Reports with Recommendations for the 510(k) Premarket Notification Process
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.