FDA Adverse Event Other Summary report: N

COR19000306-000

MDR report key: 8750184 · Received July 1, 2019

Report

Report Number
COR19000306-000
Event Type
Other
Date Received
July 1, 2019
Report Date
June 28, 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
540548 RCG

Patients

Seq Age Sex Outcome Treatment
1 Other