FDA Adverse Event Other Summary report: N

COR23000090-000

MDR report key: 16844993 · Received May 1, 2023

Report

Report Number
COR23000090-000
Event Type
Other
Date Received
May 1, 2023
Report Date
May 1, 2023
Manufacturer
Chronos Imaging, LLC
Product Code
ITY
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2321088 ITY

Patients

Seq Age Sex Outcome Treatment
1 Other