FDA Adverse Event Other Summary report: N

COR14000012-000

MDR report key: 3558089 · Received January 6, 2014

Report

Report Number
COR14000012-000
Event Type
Other
Date Received
January 6, 2014
Report Date
December 19, 2013
Product Code
RDA
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
5234 RDA

Patients

Seq Age Sex Outcome Treatment
1