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FDA 510(k) Applications Submitted by JOLIFE AB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K053403
12/06/2005
LUCAS
JOLIFE AB
K090422
02/18/2009
LUCAS 2
JOLIFE AB
K062401
08/16/2006
MODIFICATION TO LUCAS
JOLIFE AB
K161768
06/27/2016
LUCAS 3 Chest Compression System
Jolife AB
K173553
11/16/2017
LUCAS 3 Chest Compression System
Jolife AB
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