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FDA 510(k) Applications Submitted by VISIONSENSE, LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081102
04/17/2008
VSU - VISIONSENSE STEREOSCOPIC VISION SYSTEM
VISIONSENSE, LTD.
K131434
05/17/2013
VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
VISIONSENSE, LTD.
K082355
08/15/2008
VISIONSENSE STEREOSCOPIC VISION SYSTEM
VISIONSENSE, LTD.
K082667
09/12/2008
VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)
VISIONSENSE, LTD.
K123467
11/09/2012
VS3
VISIONSENSE, LTD.
K073279
11/21/2007
VS-VISIONSENSE STEREOSCOPIC VISION SYSTEM
VISIONSENSE, LTD.
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