FDA Adverse Event
Malfunction
Summary report: N
COR20000155-000
MDR report key: 10211382
·
Received June 29, 2020
Report
- Report Number
- COR20000155-000
- Event Type
- Malfunction
- Date Received
- June 29, 2020
- Report Date
- June 29, 2020
- Manufacturer
- Diode Laser Concepts, Inc.
- Product Code
- RFK
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OR, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 668637 | RFK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |