Event : Device Changes, FDA Changes, and the 510(k) - Webinar by GlobalCompliancePanel http://www.rsc.org/events/detail/4851/Device%20Changes%2c%20FDA%20Changes%2c%20and%20the%20510(k)%20-%20Webinar%20by%20GlobalCompliancePanel This is a feed for event : Device Changes, FDA Changes, and the 510(k) - Webinar by GlobalCompliancePanel Thu, 11 Sep 2014 13:13:13 +0100 4851 4851 http://www.rsc.org/events/detail/4851/Device%20Changes%2c%20FDA%20Changes%2c%20and%20the%20510(k)%20-%20Webinar%20by%20GlobalCompliancePanel Device Changes, FDA Changes, and the 510(k) - Webinar by GlobalCompliancePanel Event dates: 3 November 2010<br/>Event summary: The majority of medical devices are cleared for marketing in the U.S. by the FDA under the 510(k) process. The FDA holds companies responsible for filing new 510(k)s when one change is major enou<br/>Event Venue: Online Training Webinar, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00