Medical Devices and Diagnostic Products Standards Survey
Author :
Publisher :
Page : 232 pages
File Size : 46,13 MB
Release : 1976
Category : Medical instruments and apparatus
ISBN :
Bureau of Medical Devices Standards Survey
Author : United States. Bureau of Medical Devices
Publisher :
Page : 240 pages
File Size : 13,22 MB
Release : 1977
Category : Medical instruments and apparatus
ISBN :
Book Description
Medical devices and diagnostic products
Author :
Publisher :
Page : 172 pages
File Size : 39,67 MB
Release : 1976
Category : Medical instruments and apparatus
ISBN :
Book Description
Medical Device and Diagnostic Products Standards Survey
Author : United States. Bureau of Medical Devices and Diagnostic Products
Publisher :
Page : pages
File Size : 29,89 MB
Release : 1900
Category : Medical instruments and apparatus
ISBN :
Book Description
Standards Survey
Author : United States. Bureau of Medical Devices
Publisher :
Page : 230 pages
File Size : 39,88 MB
Release : 1976
Category : Medical instruments and apparatus
ISBN :
Book Description
Bureau of Medical Devices Standards Survey
Author :
Publisher :
Page : 156 pages
File Size : 12,90 MB
Release : 1978
Category : Medical instruments and apparatus
ISBN :
Book Description
Medical Device and Diagnostic Products Standards Survey
Author : United States. Food and Drug Administration. Bureau of Medical Devices and Diagnostic Products. Division of Medical Device Standards and Research
Publisher :
Page : pages
File Size : 38,34 MB
Release : 1976
Category : Medical instruments and apparatus
ISBN :
Book Description
Medical Device and Diagnostic Products Standard Survey
Author : United States. Bureau of Medical Devices and Diagnostic Products
Publisher :
Page : pages
File Size : 16,98 MB
Release : 1976
Category :
ISBN :
Book Description
Technological Innovation
Author : Annetine C. Gelijns
Publisher : National Academies
Page : 78 pages
File Size : 37,35 MB
Release : 1989
Category : Clinical medicine
ISBN :
Book Description
Public Health Effectiveness of the FDA 510(k) Clearance Process
Author : Institute of Medicine
Publisher : National Academies Press
Page : 141 pages
File Size : 17,50 MB
Release : 2010-10-04
Category : Medical
ISBN : 0309162904
Book Description
The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation. This document summarizes the workshop.
