FDA Adverse Event Malfunction Summary report: N

1043572-2002-00005

MDR report key: 428060 · Received November 1, 2002

Report

Report Number
1043572-2002-00005
Event Type
Malfunction
Date Received
November 1, 2002
Date of Event
September 30, 2002
Product Code
FPO
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1