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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameLADARVISION 4000 EXCIMER LASER SYSTEM AND THE LADAR 6000 EXCIMER LASER SYSTEM
Classification Nameexcimer laser system
Generic Nameophthalmic excimer laser system
ApplicantALCON LABORATORIES,INC
PMA NumberP970043
Supplement NumberS025
Date Received02/01/2006
Decision Date07/05/2006
Product Code
LZS
Advisory Committee Ophthalmic
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - software
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for an expansion of the allowable range for the physician adjustment of defocus offset parameter for the wavefront-guided myopia and myopic astigmatism indications from +=0. 75 d to up to 1. 00 d increase (more myopic treatment) and up to 2. 50 d decrease (less myopic treatment).
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