FDA Adverse Event
Injury
Summary report: N
2017233-2006-00037
MDR report key: 680212
·
Received February 23, 2006
Report
- Report Number
- 2017233-2006-00037
- Event Type
- Injury
- Date Received
- February 23, 2006
- Date of Event
- August 25, 2005
- Product Code
- FIQ
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FIQ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |