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 February 2001.
http://www.fda.gov/cdrh/510k/sumfeb01.htmlFinal 510(k) approvals for February 2001
Mar 15, 2001
Latest in Regulatory
Recalls stable for radiation oncology tools despite tech advancements
September 18, 2026
FDA issues discussion paper on GenAI medical devices
August 18, 2026
Lantheus wins FDA approval for tau PET imaging agent
August 14, 2026


















