FDA Adverse Event
Other
Summary report: N
COR15000435-000
MDR report key: 5114656
·
Received September 30, 2015
Report
- Report Number
- COR15000435-000
- Event Type
- Other
- Date Received
- September 30, 2015
- Report Date
- September 24, 2015
- Product Code
- RDA
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 643504 | RDA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |