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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.
 
DeviceINTRAOCULAR LENS MODELS C118;C119;C138 AND C139
Classification Nameintraocular lens
Generic Nameintraocular lens
Regulation Number886.3600
Applicant
ALCON LABORATORIES
6201 s freeway
ft worth, TX 76134
PMA NumberP880010
Date Received02/16/1988
Decision Date10/05/1988
Withdrawal Date 06/23/2010
Product Code
HQL[ Registered Establishments with HQL ]
Docket Number 88M-0362
Notice Date 11/30/1988
Advisory Committee Ophthalmic
Expedited Review Granted? No
Combination Product No
Supplements: S002 S003 S004 S005 S007 S008 S010 S011 S013 
S015 S016 S017 S018 S019 
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