FDA 510(k) Applications Submitted by Televere Systems

FDA 510(k) Number Submission Date Device Name Applicant
K082623 09/09/2008 VISIX IMAGING TELEVERE SYSTEMS
K061035 04/14/2006 TIGERVIEW PROFESSIONAL TELEVERE SYSTEMS
K170975 04/03/2017 Televere Digital Imaging System Televere Systems
K172124 07/14/2017 Televere Podiatry Digital Imaging System Televere Systems


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