| K-number | K024014 |
| Device name | RANDOX RX DAYTONA |
| Applicant | Randox Laboratories, Ltd. |
| Product code | CGA |
| Device class | Class II |
| Decision date | Dec 4, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 862.1345 |
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