Final 510(k) decisions for August 2002

Sep 22, 2002
Each month the U.S. Food and Drug Administration's Center for Devices and Radiological Health (CDRH) releases a final list of devices approved for marketing in the U.S. during the previous month. The following is a list of 510(k) final decisions rendered for August 2002:

http://www.fda.gov/cdrh/510k/sumaug02.html

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