FDA Adverse Event
No answer provided
Summary report: N
COR17000835-000
MDR report key: 6977158
·
Received October 25, 2017
Report
- Report Number
- COR17000835-000
- Event Type
- No answer provided
- Date Received
- October 25, 2017
- Report Date
- October 24, 2017
- Product Code
- RCC
- Report Source
- Manufacturer report
- Reporter Location
- UT, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 754824 | RCC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |