ZOLL Medical Corporation · Class III · Cleared Feb 4, 2005
| K-number | K041892 |
| Device name | ZOLL AED PRO EXTERNAL DEFIBRILLATOR |
| Applicant | ZOLL Medical Corporation |
| Product code | MKJ |
| Device class | Class III |
| Decision date | Feb 4, 2005 |
| Decision | Substantially Equivalent |
| 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