FDA Adverse Event Other Summary report: N

COR19000404-000

MDR report key: 9070120 · Received September 16, 2019

Report

Report Number
COR19000404-000
Event Type
Other
Date Received
September 16, 2019
Report Date
August 30, 2019
Manufacturer
L3Harris 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
862490 RCE

Patients

Seq Age Sex Outcome Treatment
1 NA Other