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FDA 510(k) Applications Submitted by Eckhard Loh
FDA 510(k) Number
Submission Date
Device Name
Applicant
K201724
06/23/2020
Pentacam AXL Wave
OCULUS Optikgerate GmbH
K152311
08/14/2015
Pentacam AXL
OCULUS OPTIKGERATE GMBH
K202989
09/30/2020
Myopia Master
OCULUS OptikgerΣte GmbH
K113066
10/17/2011
CORVIS ST
OCULUS OPTIKGERATE GMBH
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