FDA Adverse Event Other Summary report: N

COR14000010-000

MDR report key: 3558078 · Received January 5, 2014

Report

Report Number
COR14000010-000
Event Type
Other
Date Received
January 5, 2014
Report Date
December 18, 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
5052 RDA

Patients

Seq Age Sex Outcome Treatment
1