The following data is part of a premarket notification filed by Sauflon Pharmaceuticals, Ltd. with the FDA for Sauflon Multipurpose Solution - No Rub.
| Device ID | K030278 |
| 510k Number | K030278 |
| Device Name: | SAUFLON MULTIPURPOSE SOLUTION - NO RUB |
| Classification | Accessories, Soft Lens Products |
| Applicant | SAUFLON PHARMACEUTICALS, LTD. 49-53 YORK ST. Twickenham, Middlesex, GB Tw1-3lp |
| Contact | Ligia Delacruz |
| Correspondent | Ligia Delacruz SAUFLON PHARMACEUTICALS, LTD. 49-53 YORK ST. Twickenham, Middlesex, GB Tw1-3lp |
| Product Code | LPN |
| CFR Regulation Number | 886.5928 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-01-27 |
| Decision Date | 2003-07-30 |
| Summary: | summary |