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

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

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

104 pages missing pub info (view editions)

nonfiction politics
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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.

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