Medical Devices and the Public's Health: The FDA 510(k) Clearance Process at 35 Years by Institute of Medicine, Board on Population Health and Public He, Committee on the Public Health Effective

Medical Devices and the Public's Health: The FDA 510(k) Clearance Process at 35 Years

Institute of Medicine, Board on Population Health and Public He, Committee on the Public Health Effective

318 pages • missing pub info (view editions)

nonfiction health technology challenging informative medium-paced
Powered by AI (Beta)
Loading...

Description

Medical devices that are deemed to have a moderate risk to patients generally cannot go on the market until they are cleared through the FDA 510(k) process. In recent years, individuals and organizations have expressed concern that the 510(k) proc...

Read more

Community Reviews

Loading...

Content Warnings

Loading...