FDA Adverse Event Injury Summary report: N

1920664-2003-00137

MDR report key: 449715 · Received March 18, 2003

Report

Report Number
1920664-2003-00137
Event Type
Injury
Date Received
March 18, 2003
Date of Event
January 28, 2003
Product Code
---
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1