FDA Adverse Event
Death
Summary report: N
8022290-2001-00003
MDR report key: 332471
·
Received May 7, 2001
Report
- Report Number
- 8022290-2001-00003
- Event Type
- Death
- Date Received
- May 7, 2001
- Date of Event
- April 10, 2001
- Product Code
- ---
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 20927 | --- |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |