FDA Adverse Event Injury Summary report: N

1920664-1997-00185

MDR report key: 83080 · Received April 11, 1997

Report

Report Number
1920664-1997-00185
Event Type
Injury
Date Received
April 11, 1997
Date of Event
March 12, 1997
Product Code
HQE
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1