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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.
 
DeviceCLASSIC SERIES TM POSTERIOR CHAMBER INTRAOCULAR
Generic Nameintraocular lens
Regulation Number886.3600
ApplicantNewlensco
1911 Walker Ave.
Monrovia, CA 91016
PMA NumberP870075
Supplement NumberS001
Date Received08/10/1988
Decision Date12/06/1989
Product Code HQL 
Advisory Committee Ophthalmic
Supplement TypePanel Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
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