FDA Adverse Event
No answer provided
Summary report: N
COR13000095-000
MDR report key: 4606028
·
Received April 15, 2013
Report
- Report Number
- COR13000095-000
- Event Type
- No answer provided
- Date Received
- April 15, 2013
- Report Date
- April 10, 2013
- Product Code
- IZO
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 160087 | IZO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |