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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NONE

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Event Type  Injury  
Event Description

Following lasik surgery, i have experienced severe dry eyes and fluctuating vision throughout the day as my intraocular pressure changes. My vision fluctuates between approx 20/60 - 20/120, requiring me to wear two different pairs of glasses depending on the time of day.

 
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Brand NameNA
Type of DeviceNONE
MDR Report Key1052147
Report NumberMW5007026
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 05/24/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received05/24/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

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