The FDA's response to the GAO's report: new effort to tighten the pre-market review process for select Class III medical devices
Health Care Law Mon
.
2009 May;2009(5):2-8.
Authors
Ji Hye Kim
1
,
Jessica Smith
,
Jason Greis
,
Kristian Werling
Affiliation
1
McGuireWoods Chicago, USA.
PMID:
19449776
No abstract available
MeSH terms
Device Approval / standards*
Equipment and Supplies / classification*
United States
United States Food and Drug Administration