Smith & Nephew Dyonics, Inc. · Class II · Cleared Aug 30, 1990
| K-number | K903193 |
| Device name | SMITH & NEPHEW DYONICS LEVELERT SYSTEM |
| Applicant | Smith & Nephew Dyonics, Inc. |
| Product code | FLN |
| Device class | Class II |
| Decision date | Aug 30, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 880.2420 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov