Final 510(k) decisions for January 2003

Feb 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 January 2003:

http://www.fda.gov/cdrh/510k/sumjan03.html.

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