FDA Adverse Event No answer provided Summary report: N

COR17000867-001

MDR report key: 7104844 · Received December 11, 2017

Report

Report Number
COR17000867-001
Event Type
No answer provided
Date Received
December 11, 2017
Report Date
December 8, 2017
Product Code
RCC
Report Source
Manufacturer report
Reporter Location
UT, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
882598 RCC

Patients

Seq Age Sex Outcome Treatment
1