Company ยท DE
Oculus Optikgerate GmbH
FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2020. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 21, 2020 | K201724 | Pentacam AXL Wave Oculus Optikgerate GmbH, DE | MXK |
| Jan 20, 2016 | K152311 | Pentacam AXL Oculus Optikgerate GmbH, DE | MXK |
| Nov 8, 2012 | K113066 | CORVIS ST Oculus Optikgerate GmbH, DE | HKX |
| Sep 11, 2008 | K073508 | PARKONE Oculus Optikgerate GmbH, DE | MXK |
| Jan 28, 2005 | K041841 | PACHYCAM Oculus Optikgerate GmbH, DE | MXK |
| Sep 16, 2003 | K030719 | PENTACAM SCHEIMPFLUG CAMERA Oculus Optikgerate GmbH | MXK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||