FDA Adverse Event Other Summary report: N

2221819-1996-00360

MDR report key: 62230 · Received January 9, 1997

Report

Report Number
2221819-1996-00360
Event Type
Other
Date Received
January 9, 1997
Date of Event
April 11, 1996
Product Code
DRT
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1