The following data is part of a premarket notification filed by Bausch & Lomb Incorporated with the FDA for Boston Bl-1000-sim08 Multi-action Solution.
| Device ID | K024289 |
| 510k Number | K024289 |
| Device Name: | BOSTON BL-1000-SIM08 MULTI-ACTION SOLUTION |
| Classification | Products, Contact Lens Care, Rigid Gas Permeable |
| Applicant | BAUSCH & LOMB INCORPORATED 1400 N GOODMAN ST. Rochester, NY 14609 |
| Contact | Jennifer B Murray |
| Correspondent | Jennifer B Murray BAUSCH & LOMB INCORPORATED 1400 N GOODMAN ST. Rochester, NY 14609 |
| Product Code | MRC |
| CFR Regulation Number | 886.5918 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-12-23 |
| Decision Date | 2003-05-02 |
| Summary: | summary |