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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