FDA Adverse Event
No answer provided
Summary report: N
COR19000283-000
MDR report key: 8684647
·
Received June 10, 2019
Report
- Report Number
- COR19000283-000
- Event Type
- No answer provided
- Date Received
- June 10, 2019
- Report Date
- April 29, 2019
- Product Code
- RBY
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 474974 | RBY |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |