The following data is part of a premarket notification filed by Alcon Laboratories, Inc. with the FDA for Centurion Vision System.
Device ID | K121555 |
510k Number | K121555 |
Device Name: | CENTURION VISION SYSTEM |
Classification | Unit, Phacofragmentation |
Applicant | ALCON LABORATORIES, INC. 15800 ALTON PARKWAY Irvine, CA 92623 |
Contact | Charles Ogbonna |
Correspondent | Charles Ogbonna ALCON LABORATORIES, INC. 15800 ALTON PARKWAY Irvine, CA 92623 |
Product Code | HQC |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-05-25 |
Decision Date | 2012-12-21 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CENTURION VISION SYSTEM 85257059 4062615 Live/Registered |
NOVARTIS AG 2011-03-03 |