FDA Adverse Event Death Summary report: N

1219930-1996-00100

MDR report key: 38213 · Received September 13, 1996

Report

Report Number
1219930-1996-00100
Event Type
Death
Date Received
September 13, 1996
Date of Event
August 16, 1996
Product Code
GCJ
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1