FDA Adverse Event No answer provided Summary report: N

COR20000126-000

MDR report key: 10093700 · Received May 27, 2020

Report

Report Number
COR20000126-000
Event Type
No answer provided
Date Received
May 27, 2020
Report Date
May 26, 2020
Product Code
KPR
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
554184 KPR

Patients

Seq Age Sex Outcome Treatment
1