FDA Adverse Event
Death
Summary report: N
8010042-2008-00053
MDR report key: 1040169
·
Received May 2, 2008
Report
- Report Number
- 8010042-2008-00053
- Event Type
- Death
- Date Received
- May 2, 2008
- Product Code
- CBK
- PMA / PMN Number
- K063404
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CBK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |