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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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