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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: VISEX STAR 4- NO WAVEFRONT LASIK

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VISEX STAR 4- NO WAVEFRONT LASIK Back to Search Results
Event Date 03/05/2003
Event Type  Injury  
Event Description

Lasik surgery- non wavefront- roanoke, va at eye care & surgery. Adverse event- g. A. S. H. - glare- arc of light- starbursts- halos- at nighttime & in low light settings.

 
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Brand NameVISEX STAR 4- NO WAVEFRONT
Type of DeviceLASIK
MDR Report Key1224224
Report NumberMW5008909
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 11/06/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received11/06/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Other
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA? No

Patient TREATMENT DATA
Date Received: 11/06/2008 Patient Sequence Number: 1
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