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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: UNKNOWN LASIK

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UNKNOWN LASIK Back to Search Results
Event Date 04/01/2007
Event Type  Injury  
Event Description

I had lasik twice through a dr. My vision is terrible, blurred, cannot see after the sun goes down, unable to drive at night.

 
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Type of DeviceLASIK
Manufacturer (Section D)
UNKNOWN
unk
MDR Report Key1513504
Report NumberMW5013066
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 10/16/2009
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received10/16/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Is The Reporter A Health Professional? Yes

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