FDA Adverse Event Other Summary report: N

COR19000054-000

MDR report key: 8262025 · Received January 18, 2019

Report

Report Number
COR19000054-000
Event Type
Other
Date Received
January 18, 2019
Report Date
January 16, 2019
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
52490 RCG

Patients

Seq Age Sex Outcome Treatment
1 Other