| 标题 |
Use of Recalled Devices in New Device Authorizations Under the US Food and Drug Administration's 510(k) Pathway and Risk of Subsequent Recalls |
| 网址 | |
| DOI |
10.1001/jama.2022.23279
doi
|
| 其它 |
期刊:Journal of the American Medical Association (JAMA) 作者:Kushal T Kadakia; Sanket S. Dhruva; C. Caraballo; J. Ross; H. Krumholz 出版日期:2023-01-10 |
| 求助人 | |
| 下载 | 暂无链接,等待应助者上传 |
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(2025-6-4)