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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.
 
DeviceSTYLE UV40 POSTERIOR CHAMBER LENS
Generic Nameintraocular lens
Regulation Number886.3600
ApplicantCARL ZEISS MEDITEC AG
5160 Hacienda Drive
Dublin, CA 94568
PMA NumberP830056
Supplement NumberS035
Date Received01/07/1988
Decision Date05/03/1988
Withdrawal Date 10/12/2006
Product Code HQL 
Advisory Committee Ophthalmic
Supplement TypeNormal 180 Day Track
Supplement Reason Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
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