FDA 510(k) Applications Submitted by MATTI TULIKOURA

FDA 510(k) Number Submission Date Device Name Applicant
K130297 02/06/2013 SCANORA 3DX PALODEX GROUP OY
K110839 03/25/2011 SCANORA 3D SOREDEX PALODEX GROUP OY
K122018 07/10/2012 OP300 PALODEX GROUP OY
K163343 11/29/2016 Icare HOME tonometer Icare Finland Oy
K093683 11/30/2009 ORTHOPANTOMOGRAPH OP300 INSTRUMENTARIUM DENTAL, PALODEX GROUP OY
K153694 12/23/2015 Icare ic100 Icare Finland Oy


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