Conference - San Francisco, CA, United States
This Two-day course is a primer and overview to the premarket notification process, i.e., a 510(k). A 510(k) is a premarket submission made to FDA to demonstrate that your device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device that is not subject to PMA.
Organization: GlobalCompliancePanel
(Courtesy of GlobalCompliancePanel's logo, via http://bit.ly/1bFg4ep)
For more information, please visit: http://bit.ly/1bFg4ep
December, 12, 2013 - December, 13, 2013 (9:00 - 18:00)
DoubleTree by Hilton Hotel San Francisco Airport, San Francisco, California 94010, USA
Contact: Event Coordinator (support@globalcompliancepanel.com)
Phone: 8004479407
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