FDA Adverse Event
Summary report: N
8030904-1997-90001
MDR report key: 125138
·
Received September 16, 1997
Report
- Report Number
- 8030904-1997-90001
- Date Received
- September 16, 1997
- Product Code
- DXC
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DXC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |