FDA Adverse Event Other Summary report: N

COR18000629-000

MDR report key: 7345537 · Received March 16, 2018

Report

Report Number
COR18000629-000
Event Type
Other
Date Received
March 16, 2018
Report Date
March 12, 2018
Manufacturer
L3 Technologies, Inc
Product Code
RCG
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
187081 RCG

Patients

Seq Age Sex Outcome Treatment
1 Other