Medtronic Physio-Control Corp. · Class III · Cleared Aug 23, 2001
| K-number | K010918 |
| Device name | LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM |
| Applicant | Medtronic Physio-Control Corp. |
| Product code | MKJ |
| Device class | Class III |
| Decision date | Aug 23, 2001 |
| Decision | Substantially Equivalent - Subject to Tracking Reg. |
| Regulation | 870.5310 |
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