Portex , Ltd. · Class II · Cleared Dec 19, 2003
| K-number | K033084 |
| Device name | WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER |
| Applicant | Portex , Ltd. |
| Product code | MQF |
| Device class | Class II |
| Decision date | Dec 19, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 884.6110 |
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