FDA 510(k) Applications Submitted by KELLY ROWLAND

FDA 510(k) Number Submission Date Device Name Applicant
K021326 04/26/2002 VIDAS TESTOSTERONE (TES), MODEL 30 418 BIOMERIEUX, INC.
K051373 05/26/2005 CRONUS GUIDEWIRE, MODEL 001-001470-1 STEREOTAXIS, INC.
K051374 05/26/2005 CARDIODRIVE CATHETER ADVANCEMENT SYSTEM STEREOTAXIS, INC.
K003313 10/23/2000 FILAC FAS TEMP ELECTRONIC THERMOMETER THE KENDALL COMPANY


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