FDA Adverse Event Summary report: N

LASIK EYE SURGERY

MDR report key: 1060367 · Received June 13, 2008

Report

Report Number
MW4004346
Date Received
June 13, 2008
Manufacturer
*
Product Code
LZS
Report Source
Voluntary report
Reporter Location
KY, US
Reporter Occupation
PATIENT

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LASIK EYE SURGERY LASIK EYE SURGERY LZS * * *

Patients

Seq Age Sex Outcome Treatment
1 *