| http://www.w3.org/ns/prov#value | - The FDA will review safety data for the 25 remaining device types and, based on the risk level, issue regulations for each device type that either will require manufacturers to submit pre-market approval applications or will re-classify the devices into Class I or Class II. Today's announcement is the first step towards completing the review of Class III device types predating the 1976 law, as was
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