FDA Adverse Event Injury Summary report: N

9610877-1996-00007

MDR report key: 54245 · Received December 3, 1996

Report

Report Number
9610877-1996-00007
Event Type
Injury
Date Received
December 3, 1996
Date of Event
October 24, 1996
Manufacturer
ASAHI OPTICAL CO LTD. MEDICAL INSTRUMENT DIV.
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 DIV.

Patients

Seq Age Sex Outcome Treatment
1