FDA Adverse Event Injury Summary report: N

*

MDR report key: 155746 · Received March 9, 1998

Report

Report Number
9610877-1998-00001
Event Type
Injury
Date Received
March 9, 1998
Date of Event
January 26, 1998
Manufacturer
ASAHI OPTICAL CO, LTD/MEDICAL INSTRUMENT DIVISION
Product Code
FDF
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * FDF ASAHI OPTICAL CO, LTD/MEDICAL INSTRUMENT DIVISION

Patients

Seq Age Sex Outcome Treatment
1