FDA Adverse Event No answer provided Summary report: N

COR22000174-000

MDR report key: 15486952 · Received September 26, 2022

Report

Report Number
COR22000174-000
Event Type
No answer provided
Date Received
September 26, 2022
Report Date
September 12, 2022
Product Code
IZO
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1666100 IZO

Patients

Seq Age Sex Outcome Treatment
1 NA