Atlas FDA

Lumend, Inc.

11 FDA 510(k) clearances · Manufacturer

Sort:Newest firstOldest first

Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free

RecordFirmDate
MODIFICATION TO OUTBACK CATHETER (K043534)Lumend, Inc.2005-01-21
MODIFICATION TO OUTBACK CATHETER (K040771)Lumend, Inc.2004-04-23
LUMEND FRONTRUNNER CTO CATHETER AND ACCESSORIES (K033535)Lumend, Inc.2004-01-07
MODIFICATION TO OUTBACK CATHETER (K032298)Lumend, Inc.2003-08-26
LUMEND FRONTRUNNER GW CTO CATHETER (K031005)Lumend, Inc.2003-06-18
LUMEND FRONTRUNNER CTO CATHETER (K023114)Lumend, Inc.2003-01-23
MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETER (K023223)Lumend, Inc.2002-10-24
LUMEND FRONTRUNNER CTO CORONARY CATHETER (K013284)Lumend, Inc.2002-02-11
LUMEND PERCUTANEOUS CATHETER (K011562)Lumend, Inc.2002-01-16
MODIFICATION TO OUTBACK CATHETER (K014117)Lumend, Inc.2002-01-11
OUTBACK CATHETER (K001577)Lumend, Inc.2001-01-11

Track Lumend, Inc. automatically

Every clearance here is in the API, with alerts when new ones post.