Medical Device Manufacturer · US , Crofton , MD

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

18 submissions · 18 cleared · Since 2003
18
Total
18
Cleared
0
Denied

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.

FDA 510(k) Regulatory Record - Larsen & Toubro Limited
18 devices
1-18 of 18
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