FDA 510(k) Applications Submitted by FERENC DAHNER

FDA 510(k) Number Submission Date Device Name Applicant
K090455 02/23/2009 PROVOX VEGA, MODEL 8130-8135 ATOS MEDICAL AB
K151404 05/26/2015 ProTrach Dualcare ATOS MEDICAL AB
K141380 05/27/2014 PROVOX FREEHANDS FLEXIVOICE ATOS MEDICAL AB
K131947 06/27/2013 PROVOX VEGA PUNCTURE SET ATOS MEDICAL AB
K092593 08/24/2009 PROVOX ACTIVALVE (SIZE 4.5MM, 6MM, 8MM, 10MM, 12.5MM) ATOS MEDICAL AB


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