FDA Adverse Event No answer provided Summary report: N

COR17000359-000

MDR report key: 6531948 · Received April 28, 2017

Report

Report Number
COR17000359-000
Event Type
No answer provided
Date Received
April 28, 2017
Report Date
April 27, 2017
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
310057 RCG

Patients

Seq Age Sex Outcome Treatment
1