FDA Adverse Event Other Summary report: N

COR16000327-000

MDR report key: 5784118 · Received July 11, 2016

Report

Report Number
COR16000327-000
Event Type
Other
Date Received
July 11, 2016
Report Date
July 11, 2016
Product Code
RCC
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
435222 RCC

Patients

Seq Age Sex Outcome Treatment
1