FDA 510(k), K153642, DAILIES AquaComfort Plus, DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal

FDA 510(k), K153642, DAILIES AquaComfort Plus, DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal

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510(K) Number: K153642
Device Name: DAILIES AquaComfort Plus, DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal
Manufacturer: ALCON LABORATORIES, INC.
Device Classification Name: lenses, soft contact, daily wear
Regulation Number: 886.5925
Classification Product Code: LPL
Date Received: 12/21/2015
Decision Date: 01/20/2016
Regulation Medical Specialty: Ophthalmic

Total pages: 192
Fully redacted pages: 14
Content pages: 178

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