http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees
Food and Drug Administration should take steps to ensure that high risk device types are approved through the most stringent premarket review process
Food and Drug Administration should take steps to ensure that high-risk device types are approved through the most stringent premarket review process
Title from title screen (viewed Feb. 17, 2009).
Mode of access: Internet from GAO web site. Address as of 2/17/09: http://www.gao.gov/new.items/d09190.pdf ; current access available via PURL.
Medical devices : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process
United States. Government Accountability Office.