FDA Adverse Event Other Summary report: N

1831750-1997-00016

MDR report key: 122965 · Received September 24, 1997

Report

Report Number
1831750-1997-00016
Event Type
Other
Date Received
September 24, 1997
Date of Event
September 2, 1997
Product Code
FNM
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1