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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