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FDA 510(k) Applications Submitted by VIZTEK LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160810
03/24/2016
ViZion DR + Wireless
Viztek LLC
K152279
08/12/2015
ViZion DR + Wireless
VIZTEK LLC
K112661
09/13/2011
VIZION DR
VIZTEK LLC
K133139
10/17/2013
VIZION ULTRA
VIZTEK LLC
K123644
11/26/2012
VIZION + DR
VIZTEK LLC
K142919
10/08/2014
EXA
Viztek LLC
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