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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK LASER NONE

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LASIK LASER NONE Back to Search Results
Event Date 07/01/1998
Event Type  Injury  
Event Description

Loss of nighttime vision, dry eyes limiting quality of life, reduced capacity to perform job.

 
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Brand NameLASIK LASER
Type of DeviceNONE
MDR Report Key1467800
Report NumberMW5012606
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation
Type of Report Initial
Report Date 09/06/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received09/06/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? Yes
Device Operator OTHER
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? Yes

Patient TREATMENT DATA
Date Received: 09/06/2009 Patient Sequence Number: 1
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