FDA Adverse Event
Injury
Summary report: N
2182596-1997-00090
MDR report key: 73076
·
Received March 3, 1997
Report
- Report Number
- 2182596-1997-00090
- Event Type
- Injury
- Date Received
- March 3, 1997
- Product Code
- FTR
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FTR |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |