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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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