FDA Adverse Event Other Summary report: N

1824347-1997-00001

MDR report key: 77635 · Received March 12, 1997

Report

Report Number
1824347-1997-00001
Event Type
Other
Date Received
March 12, 1997
Date of Event
January 8, 1997
Product Code
GAB
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1