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FDA 510(k) Applications Submitted by KELLY J 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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