FDA Adverse Event Injury Summary report: N

2182596-1997-00088

MDR report key: 73111 · Received March 3, 1997

Report

Report Number
2182596-1997-00088
Event Type
Injury
Date Received
March 3, 1997
Date of Event
December 18, 1996
Product Code
FTR
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1