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» R Bogenschutz - Comment
R Bogenschutz - Comment
Document ID:
FDA-2011-N-0650-0002
Document Type:
Public Submission
Agency:
Food And Drug Administration
Received Date:
November 04 2011, at 12:00 AM Eastern Daylight Time
Date Posted:
December 22 2011, at 12:00 AM Eastern Standard Time
Comment Start Date:
October 17 2011, at 12:00 AM Eastern Standard Time
Comment Due Date:
January 17 2012, at 11:59 PM Eastern Standard Time
Tracking Number:
80f667ab
View Document:
This is comment on Proposed Rule
Cardiovascular Devices: Reclassification of External Pacemaker Pulse Generator Devices
View Comment
I am wondering if this will affect the recall status of affected products as well? I am assuming that safety was considered in the adjustment, however would like to see recalls of these products to be treated the same as prior.
Related Comments
Total:
3
Public Citizen - Comment
Public Submission
Posted:
02/14/2012
ID:
FDA-2011-N-0650-0003
Comment Period Closed
Jan 17,2012 11:59 PM ET
Patient, Consumer, and Public Health Coalition - Comment
Public Submission
Posted:
02/14/2012
ID:
FDA-2011-N-0650-0004
Comment Period Closed
Jan 17,2012 11:59 PM ET
R Bogenschutz - Comment
Public Submission
Posted:
12/22/2011
ID:
FDA-2011-N-0650-0002
Comment Period Closed
Jan 17,2012 11:59 PM ET
R Bogenschutz - Comment
This is comment on Proposed Rule
Cardiovascular Devices: Reclassification of External Pacemaker Pulse Generator Devices
View Comment
Related Comments
Public Submission Posted: 02/14/2012 ID: FDA-2011-N-0650-0003
Jan 17,2012 11:59 PM ET
Public Submission Posted: 02/14/2012 ID: FDA-2011-N-0650-0004
Jan 17,2012 11:59 PM ET
Public Submission Posted: 12/22/2011 ID: FDA-2011-N-0650-0002
Jan 17,2012 11:59 PM ET