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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.
 
DeviceOCUSIL(TM) CONTACT LENS
Generic NameLens, contact (other material) - daily
Regulation Number886.5916
ApplicantO.S.I. Corp.
601 Gateway Blvd.,#1050,
South San Francisco, CA 94080
PMA NumberP840050
Supplement NumberS017
Date Received08/17/1987
Decision Date09/21/1987
Reclassified Date03/04/1994
Product Code HQD 
Advisory Committee Ophthalmic
Supplement Type 30-Day Supplement
Supplement Reason Other
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
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