FDA Adverse Event
No answer provided
Summary report: N
COR22000011-000
MDR report key: 13366435
·
Received January 25, 2022
Report
- Report Number
- COR22000011-000
- Event Type
- No answer provided
- Date Received
- January 25, 2022
- Report Date
- January 25, 2022
- Product Code
- RFZ
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 830018 | RFZ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |