FDA Adverse Event Injury Summary report: N

2183460-1997-00084

MDR report key: 102989 · Received July 1, 1997

Report

Report Number
2183460-1997-00084
Event Type
Injury
Date Received
July 1, 1997
Date of Event
May 15, 1997
Product Code
LWS
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1