FDA Adverse Event Injury Summary report: N

*

MDR report key: 38223 · Received September 9, 1996

Report

Report Number
1416598-1996-00002
Event Type
Injury
Date Received
September 9, 1996
Date of Event
August 8, 1996
Product Code
KNX
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1