Medical device safety: how FDA regulates the reprocessing of supposedly single-use devices by Committee on Government Reform (house), United St Congress, United States House of Representatives

Medical device safety: how FDA regulates the reprocessing of supposedly single-use devices

Committee on Government Reform (house), United St Congress, United States House of Representatives

104 pages missing pub info (editions)

nonfiction politics
Powered by AI (Beta)
Loading...

Description

Medical device safety: how FDA regulates the reprocessing of supposedly single-use devices: hearing before the Committee on Government Reform, House of Representatives, One Hundred Ninth Congress, second session, September 26, 2006.

Community Reviews

Loading...

Content Warnings

Loading...