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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