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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.
 
DeviceLotrafilcon A and B Soft Contact Lenses
Generic NameLenses, soft contact, extended wear
Regulation Number886.5925
ApplicantAlcon Laboratories, Inc.
6201 S. Fwy.
Fort Worth, TX 76134
PMA NumberP010019
Supplement NumberS073
Date Received08/02/2019
Decision Date08/30/2019
Product Code LPM 
Advisory Committee Ophthalmic
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Qualification of a new X-Ray Photoelectron Spectrophotometer used for the measurement of lens plasma coating during in-process quality control inspection in the production of Alcon lotrafilcon A and lotrafilcon B soft contact lenses for daily and extended wear.
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