FDA Adverse Event
Other
Summary report: N
1213649-1999-00001
MDR report key: 213487
·
Received February 26, 1999
Report
- Report Number
- 1213649-1999-00001
- Event Type
- Other
- Date Received
- February 26, 1999
- Product Code
- KNW
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KNW |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |