The following data is part of a premarket notification filed by Bausch & Lomb Incorporated with the FDA for Renut Multiplus Mullti-purpose Solution.
| Device ID | K020802 |
| 510k Number | K020802 |
| Device Name: | RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION |
| Classification | Accessories, Solution, Ultrasonic Cleaners For Lenses |
| Applicant | BAUSCH & LOMB INCORPORATED 1400 N. GOODMAN ST. Rochester, NY 14603 -0450 |
| Contact | Paul G Stapleton |
| Correspondent | Paul G Stapleton BAUSCH & LOMB INCORPORATED 1400 N. GOODMAN ST. Rochester, NY 14603 -0450 |
| Product Code | LYL |
| CFR Regulation Number | 886.5928 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-03-12 |
| Decision Date | 2002-05-31 |
| Summary: | summary |