• 130 datasets found

    Publishers: Department of Health & Human Services

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    • CDRH FOIA Electronic Reading Room

      The CDRH FOIA electronic reading room contains frequently requested information via the Freedom of Information Act from the Center for Devices and Radiological Health.
    • FDA Data Inventory

      An inventory of all FDA Datasets
    • Product Classification

      This database contains medical device names and associated information developed by the Center. It includes a three letter device product code and a Device Class that refers to...
    • Abbott Infant Formula Recall

      This list includes products subject to recall since September 2010 related to infant formula distributed by Abbott. This list will be updated with publicly available information...
    • FDA Recognized Consensus Standards

      This database consists of those national and international standards recognized by FDA which manufacturers can declare conformity to and is part of the information the Center...
    • X-Ray Assembler Data

      Federal regulations require that an assembler who installs one or more certified components of a diagnostic x-ray system submit a report of assembly. This database contains the...
    • Postmarket Requirements and Commitments

      Provides information to the public on postmarket requirements and commitments. The phrase postmarket requirements and commitments refers to studies and clinical trials that...
    • NHRIC (National Health Related Items Code)

      The National Health Related Items Code (NHRIC) is a system for identification and numbering of marketed device packages that is compatible with other numbering systems such as...
    • Inspection Database

      FDA is disclosing the final inspection classification for inspections related to currently marketed FDA-regulated products. The disclosure of this information is not intended to...
    • 522 Postmarket Surveillance Studies

      The 522 Postmarket Surveillance Studies Program encompasses design, tracking, oversight, and review responsibilities for studies mandated under section 522 of the Federal Food,...
    • FDA Recognized Consensus Standards

      This database consists of those national and international standards recognized by FDA which manufacturers can declare conformity to and is part of the information the Center...
    • MedSun Reports

      The Medical Product Safety Network (MedSun) is an adverse event reporting program launched in 2002. The primary goal for MedSun is to work collaboratively with the clinical...
    • Establishment Registration & Device Listing

      This searchable database contains establishments (engaged in the manufacture, preparation, propagation, compounding, assembly, or processing of medical devices intended for...
    • 522 Postmarket Surveillance Studies

      The 522 Postmarket Surveillance Studies Program encompasses design, tracking, oversight, and review responsibilities for studies mandated under section 522 of the Federal Food,...
    • Plainview Milk Cooperative Ingredient Recall

      This list includes products subject to recall in the United States since June 2009 related to products manufactured by Plainview Milk Products Cooperative.
    • Abbott Infant Formula Recall

      This list includes products subject to recall since September 2010 related to infant formula distributed by Abbott. This list will be updated with publicly available information...
    • Study of Womens Health Across the Nation (SWAN) Data: Investigator Access

      The SWAN Coordinating Center provides SWAN data access to SWAN Investigators through the study website. The SWAN website provides access to longitudinal data describing the...
    • Pistachio Product Recalls

      This list includes food subject to recall in the United States since March 2009 related to pistachios distributed by Setton Pistachio of Terra Bella, Inc. The FDA has completed...
    • Food Recalls

      Press Releases of food recalls from industry
    • MedSun Reports

      The Medical Product Safety Network (MedSun) is an adverse event reporting program launched in 2002. The primary goal for MedSun is to work collaboratively with the clinical...