Alcon

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K063583ALCON VISION SYSTEMMay 9, 2008
K071236ALCON MULTI-PURPOSE SOLUTIONDecember 12, 2007
K040231INTELIPORT OCCLUDING DEVICEJuly 13, 2004
K031193SOFT (HYDROPHILIC) CONTACT LENS CARE SOLUTIONJuly 3, 2003
K981574OPTI-FREE EXPRESS MULTI-PURPOSE SOLUTIONJuly 6, 1998