FDA Adverse Event
Other
Summary report: N
8010047-1996-00006
MDR report key: 49460
·
Received November 14, 1996
Report
- Report Number
- 8010047-1996-00006
- Event Type
- Other
- Date Received
- November 14, 1996
- Date of Event
- October 7, 1996
- Product Code
- KTI
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KTI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |