Summary of Bills in the 100th Congress for Transitional Medical Devices Regulation
Summarizes legislation in the 100th Congress to regulate transitional medical devices, defined by FDA as in vitro diagnostic products and medical devices intended to diagnose, mitigate, treat, or prevent disease in humans or animals. Defines classification problems and reviews issues for Congress.
Saved in:
Corporate Author: | |
---|---|
Format: | Electronic eBook |
Language: | English |
Published: |
[Place of publication not identified] :
[publisher not identified],
1989.
|
Series: | CRS report.
|
Subjects: | |
Online Access: | Connect to this title via ProQuest |
System Under Maintenance
Our Library Management System is currently under maintenance.
Holdings and item availability information is currently unavailable. Please accept our apologies for any inconvenience this may cause and contact us for further assistance: