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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.
 
DeviceHYDRON SEMI SCLERAL, MINI, TORIC
Classification Namelenses, soft contact, daily wear
Generic Namelenses, soft contact, daily wear
Regulation Number886.5925
Applicant
COOPERVISION, INC.
370 woodcliff drive
suite 200
fairport, NY 14450-0000
PMA NumberP780007
Supplement NumberS005
Date Received02/01/1980
Decision Date06/05/1980
Product Code
LPL[ Registered Establishments with LPL ]
Advisory Committee Ophthalmic
Expedited Review Granted? No
Combination Product No
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