FDA Adverse Event No answer provided Summary report: N

COR20000328-000

MDR report key: 11091401 · Received December 29, 2020

Report

Report Number
COR20000328-000
Event Type
No answer provided
Date Received
December 29, 2020
Report Date
December 29, 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
1549847 KPR

Patients

Seq Age Sex Outcome Treatment
1