FDA Adverse Event No answer provided Summary report: N

COR19000279-000

MDR report key: 8676580 · Received June 6, 2019

Report

Report Number
COR19000279-000
Event Type
No answer provided
Date Received
June 6, 2019
Report Date
June 6, 2019
Product Code
EAP
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
466578 EAP

Patients

Seq Age Sex Outcome Treatment
1