FDA Adverse Event
No answer provided
Summary report: N
COR20000232-000
MDR report key: 10601288
·
Received September 29, 2020
Report
- Report Number
- COR20000232-000
- Event Type
- No answer provided
- Date Received
- September 29, 2020
- Report Date
- September 29, 2020
- Product Code
- KPR
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1062449 | KPR |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |