FDA Adverse Event
Injury
Summary report: N
1920664-2006-00050
MDR report key: 969043
·
Received May 22, 2006
Report
- Report Number
- 1920664-2006-00050
- Event Type
- Injury
- Date Received
- May 22, 2006
- Product Code
- HQC
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HQC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |