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Effective Date of Requirement for Premarket Approval: Cardiovascular Permanent Pacemaker Electrode

Document ID: FDA-2011-N-0505-0003
Document Type: Rule
Agency: Food And Drug Administration
Topics: Medical Devices
Federal Register Number: 2012-16486
CFR Citation: 21 CFR Part 870
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Details Information

Document Subtype: Notice of Final Rule
Received Date: July 06 2012, at 12:00 AM Eastern Daylight Time
Start-End Page: 39924 - 39927
Page Count: 4

Attachments:

Reference 1 Geiger Dale R ‘FY 2003 and 2004 Unit Costs for the Process of Medical Device Review September 2005

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Reference 2 U.S Department of Commerce Bureau of Economic Analysis National Income and Product Accounts Table 1 1 9

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