FDA Adverse Event
No answer provided
Summary report: N
COR16000650-000
MDR report key: 6210123
·
Received December 28, 2016
Report
- Report Number
- COR16000650-000
- Event Type
- No answer provided
- Date Received
- December 28, 2016
- Report Date
- December 23, 2016
- Product Code
- RCR
- 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 |
|---|---|---|---|---|---|---|---|
| 857905 | RCR |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |