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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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