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FDA 510(k)

AQUIFY LENS COMFORT DROPS

K-Number: K013204 · 2002-04-03

ApplicantCiba Vision Corporation
Decision Date2002-04-03
Product CodeMRC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AQUIFY LENS COMFORT DROPS is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Vision Corporation. It received FDA 510(k) clearance on 2002-04-03 under 510(k) number K013204. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUIFY LENS COMFORT DROPS?

AQUIFY LENS COMFORT DROPS is a medical device that received FDA 510(k) clearance on 2002-04-03. The listed applicant is Ciba Vision Corporation. The 510(k) number is K013204.

When did AQUIFY LENS COMFORT DROPS receive FDA 510(k) clearance?

AQUIFY LENS COMFORT DROPS received FDA 510(k) clearance on 2002-04-03, under 510(k) number K013204.

Who is the listed applicant for AQUIFY LENS COMFORT DROPS?

The FDA 510(k) record lists Ciba Vision Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AQUIFY LENS COMFORT DROPS?

The FDA product code for AQUIFY LENS COMFORT DROPS is MRC.

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Other records listing Ciba Vision Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123994DAILIES AQUACOMFORT PLUS, DAILIES AQUACOMFORT PLUS TORIC, DAILIES AQUACOMFORT PLUS MULTIFOCALK113168DAILIES TOTAL DALIES TOTAL FOR ASTIGMATISM DAILIES TOTAL MULTIFOCAL DAILIES TOTAL MULTIFOCAL TORICK083216CIBA VISION (NELFILCON A) ONE-DAY SOFT CONTACT LENSESK073459CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSESK072777CIBA VISION (NELFILCON A) ONE-DAY SOFT CONTACT LENSESK062262CIBA VISION (SIFILCON A) SPHERICAL, TORIC, MULTIFOCAL AND MULTIFOCAL TORIC DESIGNS

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Related Devices (Code: MRC)

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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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