id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
ihlr-18810	Swanson, Amanda	510(K) Clearance: Opportunities to Incentivize Medical Device Safety through Comparative Effectiveness Research	2012	58	.pdf	application/pdf	18913	777	50	FEDERAL REGULATION OF MEDICAL DEVICE SAFETY AND EFFICACY .................................. 172 ABSTRACT The Food and Drug Administration's 510(k) clearance process, which clears medical devices for marketing based on their similarity to devices already available on the market, has remained almost entirely unchanged since its creation in 1976.	cache/ihlr-18810.pdf	txt/ihlr-18810.txt