This page includes the latest FDA filings for Lumend Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
LUMEND, INC. | MODIFICATION TO OUTBACK CATHETER | 2004-04-23 |
LUMEND, INC. | LUMEND FRONTRUNNER CTO CATHETER AND ACCESSORIES | 2004-01-07 |
LUMEND, INC. | MODIFICATION TO OUTBACK CATHETER | 2003-08-26 |
LUMEND, INC. | LUMEND FRONTRUNNER GW CTO CATHETER | 2003-06-18 |
LUMEND, INC. | LUMEND FRONTRUNNER CTO CATHETER | 2003-01-23 |
LUMEND, INC. | MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETER | 2002-10-24 |
LUMEND, INC. | LUMEND FRONTRUNNER CTO CORONARY CATHETER | 2002-02-11 |
LUMEND, INC. | LUMEND PERCUTANEOUS CATHETER | 2002-01-16 |
LUMEND, INC. | MODIFICATION TO OUTBACK CATHETER | 2002-01-11 |
LUMEND, INC. | OUTBACK CATHETER | 2001-01-11 |
NCAGE Code | 3DCR1 | LUMEND INC |
CAGE Code | 3DCR1 | LUMEND, INC |
DUNS | 036376689 | LUMEND, INC |
SEC | 0001127101 | LUMEND INC |