Lumend, Inc.
Lumend, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2005.
Top product codes for Lumend, Inc.
Recent clearances by Lumend, Inc.
- K043534 — MODIFICATION TO OUTBACK CATHETER
- K040771 — MODIFICATION TO OUTBACK CATHETER
- K033535 — LUMEND FRONTRUNNER CTO CATHETER AND ACCESSORIES
- K032298 — MODIFICATION TO OUTBACK CATHETER
- K031005 — LUMEND FRONTRUNNER GW CTO CATHETER
- K023114 — LUMEND FRONTRUNNER CTO CATHETER
- K023223 — MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETER
- K013284 — LUMEND FRONTRUNNER CTO CORONARY CATHETER
- K011562 — LUMEND PERCUTANEOUS CATHETER
- K014117 — MODIFICATION TO OUTBACK CATHETER
- K001577 — OUTBACK CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.