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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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