eLaws
|
eCases
|
United States Code
|
Federal Courts
|
Sign In
Sign Up
eLaws
eCases »
United States Code
Federal Courts »
Home
»
Rulemaking
» Effective Date of Requirement for Premarket Approval for an Implantable Pacemaker Pulse Generator
Effective Date of Requirement for Premarket Approval for an Implantable Pacemaker Pulse Generator
Document ID:
FDA-2011-N-0522-0001
Document Type:
Proposed Rule
Agency:
Food And Drug Administration
Topics:
Medical Devices
Federal Register Number:
2011-18957
CFR Citation:
21 CFR Part 870
View Document:
Details Information
Document Subtype:
Notice of Proposed Rulemaking (NPRM)
Received Date:
July 27 2011, at 12:00 AM Eastern Daylight Time
Start-End Page:
44872 - 44877
Page Count:
6
Comment Start Date:
July 27 2011, at 12:00 AM Eastern Standard Time
Comment Due Date:
October 25 2011, at 11:59 PM Eastern Standard Time
Comments
Total:
1
National Research Center for Women & Families / Cancer Prevention and Treatment Fund - Comment
Posted:
11/22/2011
ID:
FDA-2011-N-0522-0002
Comment Period Closed
Oct 25,2011 11:59 PM ET
Related Documents
More
Total:
14
Cardiovascular Devices; Reclassification of Intra-Aortic Balloon and Control Systems (IABP) for Acute Coronary Syndrome, Cardiac and Non-Cardiac Surgery, or Complications of Heart Failure; Effective Date of Requirement for Premarket Approval for IABP for Other Specific Intended Uses
Cardiovascular Devices; Reclassification of External Counter-Pulsating Devices for Treatment of Chronic Stable Angina; Effective Date of Requirement for Premarket Approval for External Counter-Pulsating Devices for Other Specified Intended Uses
Effective Dates of Requirements for Premarket Approvals: Automated External Defibrillator System
Cardiovascular Devices; Reclassification of External Cardiac Compressor
Effective Date of Requirement for Premarket Approval: Cardiovascular Permanent Pacemaker Electrode
Effective Date Requirement for Premarket Approval for a Pacemaker Programmer
Effective Date Requirement for Premarket Approval for an Implantable Pacemaker Pulse Generator
Medical Devices: Cardiovascular Devices; Classification of Endovascular Suturing System
Cardiovascular Devices: Reclassification of External Pacemaker Pulse Generator Devices
Effective Date of Requirement for Premarket Approval for Cardiovascular Permanent Pacemaker Electrode; Correction
Requirement for Premarket Approval for Cardiovascular Permanent Pacemaker Electrode
Effective Date of Requirement for Premarket Approval for a Pacemaker Programmer
Cardiovascular Devices: Classification of Electrocardiograph Electrodes
Cardiovascular Devices: Reclassification of Certain Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheters
Effective Date of Requirement for Premarket Approval for an Implantable Pacemaker Pulse Generator
Details Information
Comments
Posted: 11/22/2011 ID: FDA-2011-N-0522-0002
Oct 25,2011 11:59 PM ET
Related Documents
More