FDA Adverse Event Injury Summary report: N

1213643-2002-00057

MDR report key: 428348 · Received November 14, 2002

Report

Report Number
1213643-2002-00057
Event Type
Injury
Date Received
November 14, 2002
Product Code
FTL
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1