FDA Adverse Event Other Summary report: N

COR19000254-000

MDR report key: 8605098 · Received May 13, 2019

Report

Report Number
COR19000254-000
Event Type
Other
Date Received
May 13, 2019
Report Date
May 8, 2019
Manufacturer
L3 Technologies, Inc
Product Code
RCE
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
395842 RCE

Patients

Seq Age Sex Outcome Treatment
1 Other