Dideco S.R.L. · Class II · Cleared Mar 8, 2005
| K-number | K050447 |
| Device name | PERFORMA ADULT HOLLOW FIBER MEMBRANE OXYGENATOR |
| Applicant | Dideco S.R.L. |
| Product code | DTZ |
| Device class | Class II |
| Decision date | Mar 8, 2005 |
| 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