FDA Adverse Event Other Summary report: N

COR14000446-000

MDR report key: 5032574 · Received October 15, 2014

Report

Report Number
COR14000446-000
Event Type
Other
Date Received
October 15, 2014
Report Date
October 9, 2014
Product Code
RCE
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
652978 RCE

Patients

Seq Age Sex Outcome Treatment
1