FDA Adverse Event Other Summary report: N

COR16000508-001

MDR report key: 6051613 · Received October 24, 2016

Report

Report Number
COR16000508-001
Event Type
Other
Date Received
October 24, 2016
Report Date
October 20, 2016
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
700831 RCG

Patients

Seq Age Sex Outcome Treatment
1