Alcon
Alcon appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 9, 2008.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K063583 | ALCON VISION SYSTEM | May 9, 2008 |
| K071236 | ALCON MULTI-PURPOSE SOLUTION | December 12, 2007 |
| K040231 | INTELIPORT OCCLUDING DEVICE | July 13, 2004 |
| K031193 | SOFT (HYDROPHILIC) CONTACT LENS CARE SOLUTION | July 3, 2003 |
| K981574 | OPTI-FREE EXPRESS MULTI-PURPOSE SOLUTION | July 6, 1998 |