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
RBMA sends commentary to CMS on MPFS Proposed Rule
September 9, 2025
Telix, FDA agree on NDA resubmission path for Pixclara
September 9, 2025