FDA Adverse Event No answer provided Summary report: N

COR08000120-000

MDR report key: 4673351 · Received March 17, 2008

Report

Report Number
COR08000120-000
Event Type
No answer provided
Date Received
March 17, 2008
Report Date
March 17, 2008
Product Code
RCS
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
1 RCS

Patients

Seq Age Sex Outcome Treatment
1