FDA Adverse Event Other Summary report: N

COR20000112-000

MDR report key: 9983324 · Received April 21, 2020

Report

Report Number
COR20000112-000
Event Type
Other
Date Received
April 21, 2020
Report Date
April 17, 2020
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
443616 RCE

Patients

Seq Age Sex Outcome Treatment
1 NA Other