FDA Adverse Event Injury Summary report: N

1221934-1997-00034

MDR report key: 133407 · Received November 13, 1997

Report

Report Number
1221934-1997-00034
Event Type
Injury
Date Received
November 13, 1997
Date of Event
October 15, 1997
Product Code
JDR
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1