FDA Adverse Event
No answer provided
Summary report: N
COR21000122-000
MDR report key: 11724641
·
Received April 23, 2021
Report
- Report Number
- COR21000122-000
- Event Type
- No answer provided
- Date Received
- April 23, 2021
- Report Date
- April 22, 2021
- Product Code
- KPR
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 608697 | KPR |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |