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How to Get Information from CDRH |
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The Freedom of Information Act (FOIA) requires federal agencies to disclose records requested in writing by any person. However, federal agencies may withhold information pursuant to nine exemptions and three exclusions which are contained in the statute. Each federal agency is responsible for meeting its FOIA responsibilities for its own records.
CDRH makes a variety of information available through its Internet site. Before CDRH created this site, much of the information could only be obtained by submitting a FOIA request and paying certain fees. Before you submit a FOIA request, please check our website. If the information you need is available, you can save time and money.
Some types of information may be viewed by simply clicking on a link. Other information requires a search: you specify certain criteria to describe the information you need and retrieve either the information or a set of links leading to the information.
| Type of Information | Format |
|---|---|
| Releasable 510(k)s | Searchable and ZIP |
| Releasable PMAs | Searchable and ZIP |
| 510(k) Summaries | Searchable |
| Product Code Data | Searchable and ZIP |
| Adverse Events | Some Searchable and ZIP |
| Registration and Listing Data | Searchable and ZIP |
| Certified Mammography Facilities | Searchable |
| Blue Book Memoranda | Viewable Directly |
| Guidance Documents | Searchable |
| NHRIC Data | Searchable |
| FDA Recognized Consensus Standards | Searchable |
| CLIA | Some Viewable Directly |
| X-Ray Assembler | Searchable and ZIP |
Note: Some information is stored as PDF files which require Acrobat Reader. ZIP files, which contain very lengthy source material compressed to enable rapid transmission, require unzip software.
Certain materials about CDRH-related matters for public distribution (e.g., press releases, consumer publications, speeches, congressional testimony) are available from the FDA Internet site. Some materials are also available locally from the more than 40 FDA public affairs specialists throughout the United States.
FDA also maintains accessible "electronic reading rooms" with agency FOIA response materials and other information routinely available to the public, with electronic search and indexing features.
If the information you seek is not available from any of the above sources, you must submit a written Freedom of Information Act (FOIA) request to FDA. CDRH is not able to accept FOIA requests via E-mail.
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