FDA 510(k) Applications Submitted by UNISENSE FERTILITECH A/S

FDA 510(k) Number Submission Date Device Name Applicant
K133712 12/05/2013 EMBRYOVIEWER SOFTWARE UNISENSE FERTILITECH A/S
K111715 06/20/2011 EMBRYOSCOPE UNISENSE FERTILITECH A/S
K092183 07/21/2009 EMBRYOSCOPE AND EMBRYOSLIDE UNISENSE FERTILITECH A/S
K113075 10/17/2011 EMBRYO VIEWER SOFTWARE UNISENSE FERTILITECH A/S


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