FDA Adverse Event
Other
Summary report: N
8010374-2005-00002
MDR report key: 667272
·
Received January 18, 2006
Report
- Report Number
- 8010374-2005-00002
- Event Type
- Other
- Date Received
- January 18, 2006
- Product Code
- FHQ
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FHQ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |