FDA Adverse Event Injury Summary report: N

1020279-1997-00040

MDR report key: 125449 · Received October 7, 1997

Report

Report Number
1020279-1997-00040
Event Type
Injury
Date Received
October 7, 1997
Date of Event
August 29, 1997
Product Code
MQZ
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1