FDA Adverse Event Other Summary report: N

COR19000406-000

MDR report key: 9075838 · Received September 17, 2019

Report

Report Number
COR19000406-000
Event Type
Other
Date Received
September 17, 2019
Report Date
September 3, 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
868028 RCE

Patients

Seq Age Sex Outcome Treatment
1 NA Other