FDA Adverse Event
No answer provided
Summary report: N
COR21000253-000
MDR report key: 14603935
·
Received August 20, 2021
Report
- Report Number
- COR21000253-000
- Event Type
- No answer provided
- Date Received
- August 20, 2021
- Report Date
- August 19, 2021
- Product Code
- RFC
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1243719 | RFC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |