FDA Adverse Event
Malfunction
Summary report: N
1920664-1997-00459
MDR report key: 125350
·
Received October 8, 1997
Report
- Report Number
- 1920664-1997-00459
- Event Type
- Malfunction
- Date Received
- October 8, 1997
- Date of Event
- August 27, 1997
- Product Code
- HQE
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HQE | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |