FDA Adverse Event Other Summary report: N

COR24000015-000

MDR report key: 18562583 · Received January 18, 2024

Report

Report Number
COR24000015-000
Event Type
Other
Date Received
January 18, 2024
Report Date
January 18, 2024
Product Code
MKB
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
9053 MKB

Patients

Seq Age Sex Outcome Treatment
1 NA Other