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

FDA 510(k) Number Submission Date Device Name Applicant
K130234 01/30/2013 NUVON VITALS CHARTING SYSTEM NUVON, INC.
K102135 07/29/2010 VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM NUVON, INC.


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