FDA Adverse Event
No answer provided
Summary report: N
COR16000620-000
MDR report key: 6166894
·
Received December 12, 2016
Report
- Report Number
- COR16000620-000
- Event Type
- No answer provided
- Date Received
- December 12, 2016
- Report Date
- December 9, 2016
- Product Code
- RCA
- 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 |
|---|---|---|---|---|---|---|---|
| 816273 | RCA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |