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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DevicePOSTERIOR CHAMBER INTRAOCULAR LENSES
Classification Nameintraocular lens
Generic Nameintraocular lens
Regulation Number886.3600
Applicant
ALCON LABORATORIES
6201 s freeway
ft worth, TX 76134
PMA NumberP810018
Supplement NumberS011
Date Received11/01/1985
Decision Date06/11/1986
Product Code
HQL[ Registered Establishments with HQL ]
Advisory Committee Ophthalmic
Expedited Review Granted? No
Combination Product No
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