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Oculus Optikgerate GmbH

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2020-10-21
TypeNumberDevice NameCodeDateActions
510(k) K201724 Pentacam AXL WaveMXK2020-10-21 View
510(k) K152311 Pentacam AXLMXK2016-01-20 View
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