| http://www.w3.org/ns/prov#value | - This morning's Washington Post, among other places, reports that there is a movement afoot to cause the FDA to review all high-risk medical devices through pre-market approval, rather than the less rigorous pre-market notification (or 510(k)) process.he is a mixed bag.This would surely increase the time it takes to get new devices on the market, which could, in some cases, hurt the public health
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