FDA Adverse Event Other Summary report: N

1831750-1998-00010

MDR report key: 180813 · Received August 3, 1998

Report

Report Number
1831750-1998-00010
Event Type
Other
Date Received
August 3, 1998
Date of Event
June 1, 1998
Product Code
FNJ
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1