FDA 510(k) Applications Submitted by OCULUS Optikgerate GmbH

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
K113066 10/17/2011 CORVIS ST OCULUS OPTIKGERATE GMBH
K041841 07/08/2004 PACHYCAM OCULUS OPTIKGERATE GMBH
K073508 12/13/2007 PARKONE OCULUS OPTIKGERATE GMBH
K030719 03/07/2003 PENTACAM SCHEIMPFLUG CAMERA OCULUS OPTIKGERATE GMBH


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