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Medical Devices: General Hospital and Personal Use Monitoring Devices; Classification of the Ingestible Event Marker

Document ID: FDA-2013-M-0042-0001
Document Type: Rule
Agency: Food And Drug Administration
Topics: Medical Devices
Federal Register Number: 2013-11628
CFR Citation: 21 CFR Part 880
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Details Information

Document Subtype: Final Rule
Received Date: May 16 2013, at 12:00 AM Eastern Daylight Time
Start-End Page: 28733 - 28735
Page Count: 3

Attachments:

Index

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Reference 1 Petition Request for Evaluation of Automatic Class III Designation Under Section 513 f 2 of the Federal Food Drug and Cosmetic Act From Proteus Biomedical Inc dated May 9 2012

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