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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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