FDA Adverse Event Injury Summary report: N

2182596-1997-00102

MDR report key: 73086 · Received March 3, 1997

Report

Report Number
2182596-1997-00102
Event Type
Injury
Date Received
March 3, 1997
Date of Event
January 10, 1997
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