FDA Adverse Event Injury Summary report: N

6000026-2000-00004

MDR report key: 269501 · Received March 10, 2000

Report

Report Number
6000026-2000-00004
Event Type
Injury
Date Received
March 10, 2000
Date of Event
January 24, 2000
Product Code
LWQ
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1