FDA Adverse Event No answer provided Summary report: N

COR20000318-000

MDR report key: 11042175 · Received December 3, 2020

Report

Report Number
COR20000318-000
Event Type
No answer provided
Date Received
December 3, 2020
Report Date
December 1, 2020
Product Code
REA
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1402363 REA

Patients

Seq Age Sex Outcome Treatment
1