FDA Adverse Event No answer provided Summary report: N

COR21000124-000

MDR report key: 11731529 · Received April 26, 2021

Report

Report Number
COR21000124-000
Event Type
No answer provided
Date Received
April 26, 2021
Report Date
April 26, 2021
Product Code
RCR
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
618440 RCR

Patients

Seq Age Sex Outcome Treatment
1