FDA Adverse Event No answer provided Summary report: N

COR19000152-000

MDR report key: 8434019 · Received March 19, 2019

Report

Report Number
COR19000152-000
Event Type
No answer provided
Date Received
March 19, 2019
Report Date
March 18, 2019
Product Code
OAP
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
224246 OAP

Patients

Seq Age Sex Outcome Treatment
1