| K-number | K030218 |
| Device name | PER, MODEL MEMO |
| Applicant | Medical Monitors Pty., Ltd. |
| Product code | DXH |
| Device class | Class II |
| Decision date | Jun 23, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 870.2920 |
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