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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 supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
DevicePOLYMETHYLMETHACRYLATE POSTERIOR CHAMBER INTR. LEN
Classification Nameintraocular lens
Generic Nameintraocular lens
Regulation Number886.3600
Applicant
ALCONRESEARCH,LTD.
6201 south freeway
fort worth,, TX 76134
PMA NumberP830040
Supplement NumberS015
Date Received07/05/1990
Decision Date12/05/1990
Product Code
HQL[ Registered Establishments with HQL ]
Advisory Committee Ophthalmic
Supplement Typenormal 180 day track
Supplement Reason location change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product No
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