FDA Adverse Event Injury Summary report: N

1920664-1996-00810

MDR report key: 47850 · Received November 6, 1996

Report

Report Number
1920664-1996-00810
Event Type
Injury
Date Received
November 6, 1996
Date of Event
September 25, 1996
Product Code
HQC
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1