FDA Adverse Event
No answer provided
Summary report: N
COR14000402-001
MDR report key: 5250305
·
Received November 24, 2015
Report
- Report Number
- COR14000402-001
- Event Type
- No answer provided
- Date Received
- November 24, 2015
- Report Date
- November 13, 2015
- Product Code
- REA
- Report Source
- Manufacturer report
- Reporter Location
- MD, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 775415 | REA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |