| K-number | K943349 |
| Device name | MAHURKAR DUAL LUMEN CATHETER |
| Applicant | Quinton, Inc. |
| Product code | FOZ |
| Device class | Class II |
| Decision date | Mar 22, 1995 |
| Decision | Unknown |
| Regulation | 880.5200 |
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