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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK SURGERY

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LASIK SURGERY Back to Search Results
Event Date 10/06/2008
Event Type  Injury  
Event Description

Ectasia in both eyes due to lasik surgery.

 
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Brand NameLASIK SURGERY
Type of DeviceLASIK
MDR Report Key1190204
Report NumberMW5008545
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 10/06/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received10/06/2008
Is This An Adverse Event Report? Yes
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: 10/06/2008 Patient Sequence Number: 1
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