Defibtech, LLC · Class III · Cleared Dec 13, 2012
| K-number | K121853 |
| Device name | DDU-2400/2450 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
| Applicant | Defibtech, LLC |
| Product code | MKJ |
| Device class | Class III |
| Decision date | Dec 13, 2012 |
| 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