| K-number | K823779 |
| Device name | DIALYTE |
| Applicant | Renal Dynamics, Inc. |
| Product code | KPO |
| Device class | Class II |
| Decision date | Jan 17, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 876.5820 |
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