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Effective Date Requirement for Premarket Approval for an Implantable Pacemaker Pulse Generator

Document ID: FDA-2011-N-0522-0003
Document Type: Rule
Agency: Food And Drug Administration
Topics: Medical Devices
Federal Register Number: 2012-15244
CFR Citation: 21 CFR Part 870
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Details Information

Document Subtype: Final Rule
Received Date: June 22 2012, at 12:00 AM Eastern Daylight Time
Start-End Page: 37573 - 37576
Page Count: 4

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