FDA Adverse Event
Other
Summary report: N
2242863-2000-00001
MDR report key: 278167
·
Received May 11, 2000
Report
- Report Number
- 2242863-2000-00001
- Event Type
- Other
- Date Received
- May 11, 2000
- Report Date
- May 7, 2000
- Product Code
- HKI
- Removal / Correction Number
- M9998
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HKI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |