Cordis Corp. · Class III · Cleared Jul 20, 1981
| K-number | K811691 |
| Device name | CORDIS OMNI-ARTICOR CARDIAC PACER #308 |
| Applicant | Cordis Corp. |
| Product code | DXY |
| Device class | Class III |
| Decision date | Jul 20, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 870.3610 |
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