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

MAUDE Adverse Event Report: ALCON ALCON LADARVISION 6000 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
 

ALCON ALCON LADARVISION 6000 NONE Back to Search Results
Event Date 05/18/2007
Event Type  Injury  
Event Description

Image from lasik surgery, dr. The intralase flap cutter, and the alcon 6000 laser platform. When are you going to do something about lasik surgery? how many more people are going to be hurt? dose or amount: #1. 90 seconds, left eye, #2. 81 seconds, right. Dates of use: 2007- 2008. Diagnosis or reason for use: to correct nearsightedness and irregular astigmatism. Event abated after the stopped or dose reduced? #1 and #2. No.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameALCON LADARVISION 6000
Type of DeviceNONE
Manufacturer (Section D)
ALCON
MDR Report Key1157865
Report NumberMW5008269
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 09/10/2008
2 DeviceS WERE Involved in the Event: 1   2  
1 Patient Was Involved in the Event
Date FDA Received09/10/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? Yes
Device Operator Health Professional
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? No
Is this a Reprocessed and Reused Single-Use Device? No

Patient TREATMENT DATA
Date Received: 09/10/2008 Patient Sequence Number: 1
-
-