FDA Adverse Event
Malfunction
Summary report: N
*
MDR report key: 1240706
·
Received August 26, 2008
Report
- Report Number
- 8010042-2008-00125
- Event Type
- Malfunction
- Date Received
- August 26, 2008
- Manufacturer
- *
- 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 |