Science Researcher Update

2-day In-person Seminar: How to Prepare & Submit a Bullet Proof 510(k) & Latest FDA Proposed Changes to the Process

Written by BCI Staff | Nov 16, 2013 9:35:00 AM

How to Prepare and Submit a Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process: 2-day In-person Seminar

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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