FDA Adverse Event
Injury
Summary report: N
1718873-1997-00001
MDR report key: 138144
·
Received August 14, 1997
Report
- Report Number
- 1718873-1997-00001
- Event Type
- Injury
- Date Received
- August 14, 1997
- Date of Event
- April 11, 1997
- Product Code
- KXO
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KXO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |