FDA Adverse Event
Other
Summary report: N
COR17000414-001
MDR report key: 6739917
·
Received July 24, 2017
Report
- Report Number
- COR17000414-001
- Event Type
- Other
- Date Received
- July 24, 2017
- Report Date
- July 20, 2017
- Manufacturer
- L3 Technologies, Inc.
- Product Code
- RCG
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 515558 | RCG |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |