FDA Adverse Event Death Summary report: N

1831750-1997-00006

MDR report key: 85426 · Received April 17, 1997

Report

Report Number
1831750-1997-00006
Event Type
Death
Date Received
April 17, 1997
Date of Event
April 5, 1997
Product Code
HDD
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HDD

Patients

Seq Age Sex Outcome Treatment
1