2023 Medical Device Submissions Workshops: 510(k) and De Novo
2023 Medical Device Submissions Workshops: 510(k) and De Novo
Learn directly from FDA and industry speakers about the regulatory requirements for bringing products to market through the 510(k) and De Novo Medical Device Submissions processes.
Day One
Day Two
Speaker Presentations
Access presenter slides below and follow along as you view the recordings.
510(k) and De Novo Agenda
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