FDA Adverse Event
Other
Summary report: N
COR18000717-000
MDR report key: 7392821
·
Received April 3, 2018
Report
- Report Number
- COR18000717-000
- Event Type
- Other
- Date Received
- April 3, 2018
- Report Date
- March 30, 2018
- Manufacturer
- L3 Technologies, Inc
- Product Code
- RCG
- 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 |
|---|---|---|---|---|---|---|---|
| 234024 | RCG |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |