FDA 510(k) Applications Submitted by LUMEND, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040771 |
03/25/2004 |
MODIFICATION TO OUTBACK CATHETER |
LUMEND, INC. |
| K031005 |
03/31/2003 |
LUMEND FRONTRUNNER GW CTO CATHETER |
LUMEND, INC. |
| K011562 |
05/21/2001 |
LUMEND PERCUTANEOUS CATHETER |
LUMEND, INC. |
| K032298 |
07/25/2003 |
MODIFICATION TO OUTBACK CATHETER |
LUMEND, INC. |
| K023114 |
09/19/2002 |
LUMEND FRONTRUNNER CTO CATHETER |
LUMEND, INC. |
| K023223 |
09/27/2002 |
MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETER |
LUMEND, INC. |
| K013284 |
10/02/2001 |
LUMEND FRONTRUNNER CTO CORONARY CATHETER |
LUMEND, INC. |
| K033535 |
11/10/2003 |
LUMEND FRONTRUNNER CTO CATHETER AND ACCESSORIES |
LUMEND, INC. |
| K043534 |
12/22/2004 |
MODIFICATION TO OUTBACK CATHETER |
LUMEND, INC. |
| K001577 |
05/22/2000 |
OUTBACK CATHETER |
LUMEND, INC. |
| K014117 |
12/14/2001 |
MODIFICATION TO OUTBACK CATHETER |
LUMEND, INC. |
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