FDA Adverse Event No answer provided Summary report: N

COR22000116-000

MDR report key: 14931890 · Received July 5, 2022

Report

Report Number
COR22000116-000
Event Type
No answer provided
Date Received
July 5, 2022
Report Date
July 5, 2022
Product Code
RCG
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
366344 RCG

Patients

Seq Age Sex Outcome Treatment
1