FDA Adverse Event No answer provided Summary report: N

COR14000168-000

MDR report key: 3793611 · Received May 6, 2014

Report

Report Number
COR14000168-000
Event Type
No answer provided
Date Received
May 6, 2014
Report Date
May 2, 2014
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
269688 RDA

Patients

Seq Age Sex Outcome Treatment
1