Oculus Optikgerate GmbH

Oculus Optikgerate GmbH holds 6 FDA 510(k) medical device clearances, first cleared 2003, most recent 2020.

Top product codes for Oculus Optikgerate GmbH

MXK — Ophthalmic5 devices
HKX — Ophthalmic1 device

Recent clearances by Oculus Optikgerate GmbH

K201724 — Pentacam AXL WaveCode MXK·2020-10-21
K152311 — Pentacam AXLCode MXK·2016-01-20
K113066 — CORVIS STCode HKX·2012-11-08
K073508 — PARKONECode MXK·2008-09-11
K041841 — PACHYCAMCode MXK·2005-01-28
K030719 — PENTACAM SCHEIMPFLUG CAMERACode MXK·2003-09-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.