FDA Adverse Event Other Summary report: N

COR14000541-000

MDR report key: 4301592 · Received December 5, 2014

Report

Report Number
COR14000541-000
Event Type
Other
Date Received
December 5, 2014
Report Date
December 4, 2014
Product Code
RCG
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
785788 RCG

Patients

Seq Age Sex Outcome Treatment
1