{"title":"Device user regulations, not user friendly.","authors":"J Cooney","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The FDA invited input from healthcare organizations on the Safe Medical Devices Act of 1990, but they ended up receiving more questions than comments.</p>","PeriodicalId":79559,"journal":{"name":"AOHA : a publication of the American Osteopathic Hospital Association","volume":"35 6","pages":"4"},"PeriodicalIF":0.0000,"publicationDate":"1991-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AOHA : a publication of the American Osteopathic Hospital Association","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The FDA invited input from healthcare organizations on the Safe Medical Devices Act of 1990, but they ended up receiving more questions than comments.