FDA Adverse Event Other Summary report: N

COR20000118-000

MDR report key: 10048959 · Received May 12, 2020

Report

Report Number
COR20000118-000
Event Type
Other
Date Received
May 12, 2020
Report Date
May 8, 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
509488 RCE

Patients

Seq Age Sex Outcome Treatment
1 NA Other