FDA Adverse Event Injury Summary report: N

1220923-1997-00020

MDR report key: 123831 · Received October 1, 1997

Report

Report Number
1220923-1997-00020
Event Type
Injury
Date Received
October 1, 1997
Date of Event
February 14, 1997
Product Code
LJT
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1