| K-number | K924571 |
| Device name | MEDI-SOL |
| Applicant | Orange-Sol, Inc. |
| Product code | KOX |
| Device class | Class I |
| Decision date | Apr 6, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 878.4730 |
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