| K-number | K952810 |
| Device name | DOSI-FLOW, MODELS 20 & 30 |
| Applicant | Leventon, S.A. |
| Product code | FPA |
| Device class | Class II |
| Decision date | Sep 8, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 880.5440 |
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