Comments on: FDA plans aggressive overhaul of 510(k); unique device identifier coming in 2013 http://www.medcitynews.com/2010/01/fda-plans-agressive-overhaul-of-510k/?utm_source=rss&utm_medium=rss&utm_campaign=fda-plans-agressive-overhaul-of-510k MedCity News Sat, 11 Feb 2012 15:17:29 +0000 hourly 1 http://wordpress.org/?v=3.2.1 By: FDA Sets Goal of September, 2013, Deadline for UDI Implementation « Loftware http://www.medcitynews.com/2010/01/fda-plans-agressive-overhaul-of-510k/comment-page-1/#comment-56264 FDA Sets Goal of September, 2013, Deadline for UDI Implementation « Loftware Tue, 02 Feb 2010 14:06:19 +0000 http://www.medcitynews.com/?p=19000#comment-56264 [...] At this link you can see the FDA’s/CDRH complete FY10 planning document. There is a lot of information in the document as well about the planned overhaul of the 510(k) and pre-market approval processes. For a quick summary of the overall implications, you can read a good news overview courtesy of this MedCity News posting. [...] [...] At this link you can see the FDA’s/CDRH complete FY10 planning document. There is a lot of information in the document as well about the planned overhaul of the 510(k) and pre-market approval processes. For a quick summary of the overall implications, you can read a good news overview courtesy of this MedCity News posting. [...]

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