FDA 510(k) Applications Submitted by STEPHANIE HARRINGTON

FDA 510(k) Number Submission Date Device Name Applicant
K041077 04/26/2004 IMALUX OCT PROBE GUIDE IMALUX CORPORATION
K042894 10/20/2004 IMALUX NIRIS IMAGING SYSTEM IMALUX CORPORATION
K033783 12/04/2003 IMALUX OCT IMAGING SYSTEM IMALUX COPORATION


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