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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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