Devices
Showing 11–20 of 55 results
Your Data License
- ResearchNon-Commercial, Share-Alike, Attribution Free Forever
- CommercialCommercial Use, Remix & Adapt, White Label Log in to download
-
The Clinical Laboratory Improvement Amendments (CLIA) Dataset includes records of all commercially marketed laboratory tests categorized by CDC or FDA. For each Document Number tha...
-
This dataset is one of the surveys carried out by Dartmouth Atlas under the umbrella "Effective Care". Effective care refers to services that are of proven value and have no signif...
-
This data package contains the records of all commercially marketed laboratory tests that have been categorized under the Clinical Laboratory Improvement Amendments (CLIA), zip co...
-
This dataset is one of the surveys carried out by Dartmouth Atlas under the umbrella "Effective Care". Effective care refers to services that are of proven value and have no signif...
-
This data package contains datasets on medical device establishment including foreign firms that manufacture medical devices, registered and non-registered importers with the Foo...
-
FDA Certified Mammography Facilities dataset is updated periodically based on information received from the four FDA-approved accreditation bodies: the American College of Radiolog...
-
Premarket Approval (PMA) Summary Review Memos for 180-Day Design Changes dataset is published as part of a pilot program under the Center for Devices and Radiological Health (CDRH)...
-
A 510(k) is required when: - Introducing a device into commercial distribution (marketing) for the first time. After May 28, 1976 (effective date of the Medical Device Amendments t...
-
This data package contains the lists of medical device names and associated information developed by the Center for Devices and Radiological Health (CDRH) in support of its mission...
-
CDRH’s Post-Approval Studies Program ensures that methodologies are well-designed and conducted effectively, efficiently and in the least burdensome manner. In 2005, the Division...