FDA Adverse Event No answer provided Summary report: N

COR14000402-000

MDR report key: 4635482 · Received September 15, 2014

Report

Report Number
COR14000402-000
Event Type
No answer provided
Date Received
September 15, 2014
Report Date
September 15, 2014
Product Code
REA
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
568275 REA

Patients

Seq Age Sex Outcome Treatment
1