FDA Adverse Event
Summary report: N
1920664-1998-00163
MDR report key: 184289
·
Received August 6, 1998
Report
- Report Number
- 1920664-1998-00163
- Date Received
- August 6, 1998
- Date of Event
- June 15, 1998
- 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 |