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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK

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LASIK Back to Search Results
Event Type  Injury  
Event Description

Severe dry eyes night vision problems.

 
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Brand NameLASIK
Type of DeviceLASIK
MDR Report Key2045913
Report NumberMW5020170
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Physician
Type of Report Initial
Report Date 04/03/2011
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received04/03/2011
Is This An Adverse Event Report? No
Is This A Product Problem Report? No
Device Operator Health Professional
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 04/03/2011 Patient Sequence Number: 1
Treatment
LASIK
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