• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK SURGERY NONE

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

LASIK SURGERY NONE Back to Search Results
Event Date 01/01/2002
Event Type  Injury  
Event Description

Dry eye several years after lasik surgery. Plus, i have had halos around lights at night and especially when driving at night. Today, i read the fda plans to study the post-operative effects of lasik surgery. So, i thought i would add my adverse events after having the procedure about 10 years ago.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameLASIK SURGERY
Type of DeviceNONE
MDR Report Key1512190
Report NumberMW5013046
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 10/15/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received10/15/2009
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? Yes

Patient TREATMENT DATA
Date Received: 10/15/2009 Patient Sequence Number: 1
-
-