FDA Adverse Event
Malfunction
Summary report: N
1222166-2007-00292
MDR report key: 968850
·
Received June 7, 2007
Report
- Report Number
- 1222166-2007-00292
- Event Type
- Malfunction
- Date Received
- June 7, 2007
- Product Code
- KSZ
- PMA / PMN Number
- 103778
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KSZ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |