Oculus Optikgerate GmbH
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K201724 | Pentacam AXL Wave | October 21, 2020 |
| K152311 | Pentacam AXL | January 20, 2016 |
| K113066 | CORVIS ST | November 8, 2012 |
| K073508 | PARKONE | September 11, 2008 |
| K041841 | PACHYCAM | January 28, 2005 |
| K030719 | PENTACAM SCHEIMPFLUG CAMERA | September 16, 2003 |