eLaws | eCases | United States Code | Federal Courts |
Home » Rulemaking » Center for Devices and Radiological Health 510(k) Clearance Process; Recommendations Proposed in Institute of Medicine Report: ‘‘Medical Devices and the Public’s Health, The FDA 510(k) Clearance Process at 35 Years;’’ Public Meeting

Center for Devices and Radiological Health 510(k) Clearance Process; Recommendations Proposed in Institute of Medicine Report: ‘‘Medical Devices and the Public’s Health, The FDA 510(k) Clearance Process at 35 Years;’’ Public Meeting

Document ID: FDA-2011-N-0556-0002
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2011-20575
View Document:  View as format pdf View as format html

Details Information

Abstract: Meeting on September 16, 2011
Document Subtype: Notice of Meeting
Received Date: August 12 2011, at 12:00 AM Eastern Daylight Time
Start-End Page: 50230 - 50231
Page Count: 2
Comment Start Date: August 12 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: September 30 2011, at 11:59 PM Eastern Standard Time

Attachments:

RECOMMENDATIONS PROPOSED IN INSTITUTE OF MEDICINE REPORT MEDICAL DEVICES AND THE PUBLIC'S HEALTH, THE FDA 510(K) CLEARANCE PROCESS AT 35 YEARS

View Attachment: View as format pdf

Comments

    View All
Total: 21
Colorado Bioscience Association - Comment
Posted: 10/07/2011     ID: FDA-2011-N-0556-0013

Sep 30,2011 11:59 PM ET
Biomet, Inc. - Testimony
Posted: 10/07/2011     ID: FDA-2011-N-0556-0014

Sep 30,2011 11:59 PM ET
American College of Cardiology - Comment
Posted: 10/07/2011     ID: FDA-2011-N-0556-0015

Sep 30,2011 11:59 PM ET
Arizona Bioindustry Association - Comment
Posted: 10/07/2011     ID: FDA-2011-N-0556-0019

Sep 30,2011 11:59 PM ET
LifeScience Alley - Comment
Posted: 10/07/2011     ID: FDA-2011-N-0556-0020

Sep 30,2011 11:59 PM ET

Related Documents

Total: 0
No documents available.