FDA Adverse Event Other Summary report: N

COR18001737-000

MDR report key: 8069827 · Received November 14, 2018

Report

Report Number
COR18001737-000
Event Type
Other
Date Received
November 14, 2018
Report Date
November 9, 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
907648 RCG

Patients

Seq Age Sex Outcome Treatment
1 Other