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Record Nr. |
UNINA9910697929303321 |
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Titolo |
Medical devices [[electronic resource] ] : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees |
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Pubbl/distr/stampa |
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[Washington, D.C.] : , : U.S. Govt. Accountability Office, , [2009] |
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Descrizione fisica |
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iv, 57 pages : digital, PDF file |
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Soggetti |
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Medical instruments and apparatus - Standards - United States |
Equipment and Supplies - standards |
Statistics. |
United States |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Title from title screen (viewed Feb. 17, 2009). |
"January 2009." |
"GAO-09-190." |
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Nota di bibliografia |
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Includes bibliographical references. |
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