Medtronic Vascular · Class II · Cleared Dec 16, 1996
| K-number | K962641 |
| Device name | MAXIMA FORTE HOLLOW FIBER OXYGENATOR WITH PLASMA RESISTANT FIBER |
| Applicant | Medtronic Vascular |
| Product code | DTZ |
| Device class | Class II |
| Decision date | Dec 16, 1996 |
| Decision | Substantially Equivalent |
| Regulation | 870.4350 |
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