The following data is part of a premarket notification filed by Bausch + Lomb with the FDA for Stellaris Elite Vision Enhancement System.
Device ID | K170052 |
510k Number | K170052 |
Device Name: | Stellaris Elite Vision Enhancement System |
Classification | Unit, Phacofragmentation |
Applicant | Bausch + Lomb 3365 Tree Ct. Industrial Blvd St. Louis, MO 63122 |
Contact | Dan Regan |
Correspondent | Dan Regan Bausch + Lomb 3365 Tree Ct. Industrial Blvd St. Louis, MO 63122 |
Product Code | HQC |
Subsequent Product Code | HQE |
Subsequent Product Code | HQF |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-01-05 |
Decision Date | 2017-04-19 |
Summary: | summary |