FDA 510(k) Applications Submitted by VIZTEK, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K063337 11/06/2006 OPAL-RAD VIZTEK, INC.
K091752 06/16/2009 VIZTEK WL VIZTEK, INC.
K082604 09/08/2008 VIZTEK DR, MODELS: DR1000, DR3000, DR4000 VIZTEK, INC.
K102123 07/29/2010 VIZION DR VIZTEK, INC.
K003607 11/22/2000 ONYX-RAD TELEMEDICINE PACS VIZTEK, INC.


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