Defibtech, LLC · Class III · Cleared Jan 4, 2013
| K-number | K113787 |
| Device name | DDU-120 FULLY AUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
| Applicant | Defibtech, LLC |
| Product code | MKJ |
| Device class | Class III |
| Decision date | Jan 4, 2013 |
| 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