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How Does The FDA's New Usability Guidance Affect Your 510k submissions?
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The FDA has a great example of what I refer to as 'ease of use' at 'point of use'. If you look at Section 6.2 of their 2016 Usability Guidance Document, they suggest performing essentially a literature search to identify known use related issues for medical devices that are similar to the one that you are developing. Then, they provide seven examples such as the MAUDE and Recall databases, but they provide them as clickable hyperlinks that will bring you straight to the database in question. Thi
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