Medtronic Vascular · Class III · Cleared Jan 4, 1978
| K-number | K771786 |
| Device name | CARDIAC PULSE GENERATORS 5982/5983 |
| Applicant | Medtronic Vascular |
| Product code | DXY |
| Device class | Class III |
| Decision date | Jan 4, 1978 |
| 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