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FDA Organization
Office of Medical Products and Tobacco
About the Center for Devices and Radiological Health
CDRH Reports
CDRH Annual Reports
CDRH Preliminary Internal Evaluations
CDRH Plan of Action for 510(k) and Science
Medical Device Pre-Market Programs: An Overview of FDA Actions
Medical Device Reporting (MDR) Rate in 510(k) Cleared Devices Using Multiple Predicates
Medical Device Technology Forecasts
National Medical Device Postmarket Surveillance Plan
Office of Communication, Education and Radiation Programs Annual Reports
Office of Compliance Reports
Office of Device Evaluation Annual Reports
Office of In Vitro Diagnostic Device Evaluation and Safety Annual Reports
Office of Science and Engineering Laboratories Annual Reports
Regulatory Science Report
Reports to Congress
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Office of Communication, Education and Radiation Programs Annual Reports
Note: OCER was formerly known as the Office of Health and Industry Programs (OHIP)
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FY 2005 OCER Annual Report
FY 2003 OHIP Annual Report
FY 2001 OHIP Annual Report
FY 2000 OHIP Annual Report
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