FDA Adverse Event No answer provided Summary report: N

COR16000226-000

MDR report key: 5729019 · Received June 16, 2016

Report

Report Number
COR16000226-000
Event Type
No answer provided
Date Received
June 16, 2016
Report Date
March 8, 2016
Product Code
RCG
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
382903 RCG

Patients

Seq Age Sex Outcome Treatment
1