FDA Adverse Event
Other
Summary report: N
8010528-2007-00001
MDR report key: 980217
·
Received October 18, 2007
Report
- Report Number
- 8010528-2007-00001
- Event Type
- Other
- Date Received
- October 18, 2007
- Product Code
- LRW
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LRW |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |