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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: VISX LASER NONE

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VISX LASER NONE Back to Search Results
Event Date 07/07/1998
Event Type  Injury  
Event Description

Severe contrast, low light issues from lasik. Diagnosis or reason for use: was not evaluated completely.

 
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Brand NameVISX LASER
Type of DeviceNONE
MDR Report Key1226129
Report NumberMW5008915
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 11/09/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received11/09/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 11/09/2008 Patient Sequence Number: 1
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