FDA Adverse Event Death Summary report: N

2021283-1997-00040

MDR report key: 112214 · Received August 4, 1997

Report

Report Number
2021283-1997-00040
Event Type
Death
Date Received
August 4, 1997
Date of Event
November 15, 1996
Manufacturer
IMED CORP
Product Code
FRN
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FRN IMED CORP 1340 NA

Patients

Seq Age Sex Outcome Treatment
1