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 2001.
http://www.fda.gov/cdrh/510k/sumaug01.html
http://www.fda.gov/cdrh/510k/sumaug01.html
