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FDA 510(k)

DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal

K-Number: K172066 · 2017-08-09

ApplicantAlcon Laboratories, Inc.
Decision Date2017-08-09
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal is a medical device manufactured by Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2017-08-09 under approval number K172066. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal?

DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal is a medical device that received FDA 510(k) clearance on 2017-08-09. It is manufactured by Alcon Laboratories, Inc.. The 510(k) number is K172066.

When was DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal approved by the FDA?

DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal received FDA 510(k) clearance on 2017-08-09, under approval number K172066.

What company makes DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal?

DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal is manufactured by Alcon Laboratories, Inc..

What is the FDA product code for DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal?

The FDA product code for DAILIES AquaComfort Plus (sphere), DAILIES AquaComfort Plus Toric, DAILIES AquaComfort Plus Multifocal is LPL.

Other Devices by Alcon Laboratories, Inc.

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Related Devices (Code: LPL)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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