FDA Adverse Event
Injury
Summary report: N
1920664-2001-00001
MDR report key: 311098
·
Received January 4, 2001
Report
- Report Number
- 1920664-2001-00001
- Event Type
- Injury
- Date Received
- January 4, 2001
- Date of Event
- November 16, 2000
- Product Code
- HQC
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 502 | HQC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |