FDA Adverse Event Death Summary report: N

*

MDR report key: 1080692 · Received July 21, 2008

Report

Report Number
8010182-2008-00001
Event Type
Death
Date Received
July 21, 2008
Manufacturer
GAMBRO INDUSTRIES
Product Code
FJK
PMA / PMN Number
k032431
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * FJK GAMBRO INDUSTRIES * *

Patients

Seq Age Sex Outcome Treatment
1