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Patient, Consumer, and Public Health Coalition - Comment

Document ID: FDA-2011-N-0650-0004
Document Type: Public Submission
Agency: Food And Drug Administration
Received Date: January 17 2012, at 12:00 AM Eastern Standard Time
Date Posted: February 14 2012, 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: 80f9955f
View Document:  View as format xml

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We strongly oppose the reclassification of External Pacemaker Pulse Generator Devices from class III to class II. See attached Word document for our comments.

Attachments:

Patient, Consumer, and Public Health Coalition ReclassificationPacemakersCommentsdueJanuary171dc

Title:
Patient, Consumer, and Public Health Coalition ReclassificationPacemakersCommentsdueJanuary171dc

View Attachment: View as format msw8 View as format pdf

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