Larsen & Toubro Limited - FDA 510(k) Cleared Devices

Larsen & Toubro Limited has 18 FDA 510(k) cleared cardiovascular devices. Based in Crofton, US.

Historical record: 18 cleared submissions from 2003 to 2011.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Entela, Inc., Intertek Testing Services and Underwriters Laboratories, Inc.. 2 devices have linked clinical trials registered on ClinicalTrials.gov.