Terumo Medical Corp. · Class II · Cleared Sep 2, 1993
| K-number | K922799 |
| Device name | CAPIOX SX HOLLOW FIBER OXYGENATOR |
| Applicant | Terumo Medical Corp. |
| Product code | DTZ |
| Device class | Class II |
| Decision date | Sep 2, 1993 |
| 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