FDA Adverse Event Injury Summary report: N

1920664-2002-00002

MDR report key: 371627 · Received January 15, 2002

Report

Report Number
1920664-2002-00002
Event Type
Injury
Date Received
January 15, 2002
Date of Event
December 4, 2001
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