APA (7th ed.) Citation

Center for Devices and Radiological Health (U.S.) & Center for Biologics Evaluation and Research (U.S.). (2008). Modifications to devices subject to premarket approval (PMA): The PMA supplement decision-making process. U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health ; Center for Biologics Evaluation and Research.

Chicago Style (17th ed.) Citation

Center for Devices and Radiological Health (U.S.) and Center for Biologics Evaluation and Research (U.S.). Modifications to Devices Subject to Premarket Approval (PMA): The PMA Supplement Decision-making Process. [Silver Spring, Md.] : [Rockville, Md.]: U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health ; Center for Biologics Evaluation and Research, 2008.

MLA (9th ed.) Citation

Center for Devices and Radiological Health (U.S.) and Center for Biologics Evaluation and Research (U.S.). Modifications to Devices Subject to Premarket Approval (PMA): The PMA Supplement Decision-making Process. U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health ; Center for Biologics Evaluation and Research, 2008.