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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.
 
DeviceMETRO 55 (METHAFILCON A)
Generic NameLenses, soft contact, daily wear
Regulation Number886.5925
ApplicantMetrosoft, Inc.
P.O. Box 14847
Austin, TX 78761
PMA NumberP830077
Supplement NumberS002
Date Received10/28/1988
Decision Date03/02/1989
Product Code LPL 
Advisory Committee Ophthalmic
Supplement TypeNormal 180 Day Track
Supplement Reason Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
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