Final 510(k) decisions for December 2002

Jan 5, 2003

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 December 2002:

http://www.fda.gov/cdrh/510k/sumdec02.html.

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