| K-number | K950878 |
| Device name | MENICON SP VIAL |
| Applicant | Hyman, Phelps & McNamara, P.C. |
| Product code | LRX |
| Device class | Class II |
| Decision date | Apr 7, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 886.5928 |
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