FDA Adverse Event Other Summary report: N

COR14000287-000

MDR report key: 3900367 · Received June 27, 2014

Report

Report Number
COR14000287-000
Event Type
Other
Date Received
June 27, 2014
Report Date
June 6, 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
375726 RDA

Patients

Seq Age Sex Outcome Treatment
1