FDA Adverse Event Injury Summary report: N

8010047-1996-00003

MDR report key: 39523 · Received September 20, 1996

Report

Report Number
8010047-1996-00003
Event Type
Injury
Date Received
September 20, 1996
Report Date
September 20, 1996
Manufacturer
OLYMPUS OPTICAL CO. LTD.
Product Code
KOG
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 KOG OLYMPUS OPTICAL CO. LTD.

Patients

Seq Age Sex Outcome Treatment
1 *