FDA 510(k) Applications Submitted by CANDELIS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K092949 09/24/2009 IMAGEGRID RADIOLOGY VIEWER SYSTEM CANDELIS, INC.
K080333 02/07/2008 IMAGEGRID CANDELIS, INC.
K111694 06/16/2011 ASTRA CANDELIS, INC.


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