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Start Over Subjects Humans ✖Remove constraint Subjects: Humans Subjects Clinical Trials as Topic ✖Remove constraint Subjects: Clinical Trials as Topic Titles Appropriate use of voluntary consensus standards in premarket submissions for medical devices: guidance for industry and Food and Drug Administration staff ✖Remove constraint Titles: Appropriate use of voluntary consensus standards in premarket submissions for medical devices: guidance for industry and Food and Drug Administration staff Dates by Range 2000 and later ✖Remove constraint Dates by Range: 2000 and later

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  • Appropriate use of voluntary consensus standards in premarket submissions for medical devices: guidance for industry and Food and Drug Administration staff1