FDA Adverse Event Other Summary report: N

1519132-1996-00002

MDR report key: 49415 · Received November 13, 1996

Report

Report Number
1519132-1996-00002
Event Type
Other
Date Received
November 13, 1996
Date of Event
March 30, 1996
Product Code
FFK
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1