The 510(k) Submission: Requirements, Contents, and Options 2013 2013 is a webinar that covers topics such as:
The 510(k) Submission: Requirements, Contents, and Options 2013 2013 brings together attendees from medical device companies, including Regulatory management, Executive management, R&D personnel involved in approving the design of medical devices, Professionals involved with premarket notification to the FDA and Sales personnel involved in approving the marketing of medical devices.