FDA Adverse Event Other Summary report: N

COR18000015-001

MDR report key: 7241685 · Received February 5, 2018

Report

Report Number
COR18000015-001
Event Type
Other
Date Received
February 5, 2018
Report Date
February 1, 2018
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
83637 RCG

Patients

Seq Age Sex Outcome Treatment
1 Other