FDA Adverse Event Other Summary report: N

COR15000350-000

MDR report key: 4997194 · Received August 12, 2015

Report

Report Number
COR15000350-000
Event Type
Other
Date Received
August 12, 2015
Report Date
August 11, 2015
Product Code
RCA
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
527718 RCA

Patients

Seq Age Sex Outcome Treatment
1