FDA Adverse Event
Malfunction
Summary report: N
8010177-1996-00015
MDR report key: 76600
·
Received November 26, 1996
Report
- Report Number
- 8010177-1996-00015
- Event Type
- Malfunction
- Date Received
- November 26, 1996
- Date of Event
- October 14, 1996
- Product Code
- HXX
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HXX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |