Alcon Manufacturing, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K120912 | INFINITI(R) VISION SYSTEM | June 15, 2012 |
| K112425 | INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE | November 21, 2011 |
| K101774 | MONARCH III IOL DELIVERY SYSTEM; MONARCH III P CATRIDGE; MONARCH III HANDPIECE (H4) | October 13, 2011 |
| K101285 | CONSTELLATION VISION SYSTEM | November 12, 2010 |
| K093210 | AQUALASE CAPSULE WASH TIP | March 4, 2010 |
| K063155 | MONARCH III IOL DELIVERY SYSTEM | March 27, 2007 |