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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK EYE SURGERY

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LASIK EYE SURGERY Back to Search Results
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Brand NameLASIK EYE SURGERY
Type of DeviceLASIK EYE SURGERY
MDR Report Key1060367
Report NumberMW4004346
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received06/13/2008
Is This An Adverse Event Report? No
Is This A Product Problem Report?
Device Operator Invalid Data
Was Device Available For Evaluation? No Answer Provided
Is The Reporter A Health Professional? No Answer Provided
Was the Report Sent to FDA? No
Event Location Home
Is this a Reprocessed and Reused Single-Use Device? No

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