FDA Adverse Event No answer provided Summary report: N

COR20000296-000

MDR report key: 10903397 · Received November 19, 2020

Report

Report Number
COR20000296-000
Event Type
No answer provided
Date Received
November 19, 2020
Report Date
November 19, 2020
Product Code
KPR
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1330682 KPR

Patients

Seq Age Sex Outcome Treatment
1