FDA Adverse Event Injury Summary report: N

9610877-1996-00006

MDR report key: 54143 · Received December 2, 1996

Report

Report Number
9610877-1996-00006
Event Type
Injury
Date Received
December 2, 1996
Date of Event
October 14, 1996
Manufacturer
ASAHI OPTICAL CO, LTD. MEDICAL ISNTRUMENT DIV.
Product Code
FET
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FET ASAHI OPTICAL CO, LTD. MEDICAL ISNTRUMENT DIV.

Patients

Seq Age Sex Outcome Treatment
1