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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.
 
DeviceTECNIS ACRYLIC INTRAOCULAR LENS
Generic Nameintraocular lens
Regulation Number886.3600
ApplicantJohnson & Johnson Surgical Vision, Inc.
31 Technology Drive
Suite 200
Irvine, CA 92618
PMA NumberP990080
Supplement NumberS039
Date Received04/01/2015
Decision Date05/01/2015
Product Code HQL 
Advisory Committee Ophthalmic
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
IMPLEMENTATION OF A NEW METHOD FOR MEASUREMENT OF THE OPTICAL PROPERTIES(DIOPTER AND IMAGE QUALITY) OF THE 3-PIECE ACRYLIC AND SILICONE IOLS PRODUCED AT AMO¿S PUERTO RICO FACILITY.
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