FDA Adverse Event
Injury
Summary report: N
1217116-1997-00021
MDR report key: 97069
·
Received June 6, 1997
Report
- Report Number
- 1217116-1997-00021
- Event Type
- Injury
- Date Received
- June 6, 1997
- Date of Event
- April 16, 1997
- Product Code
- IZO
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | IZO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |