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FDA 510(k)

HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES

K-Number: K043540 · 2005-02-01

Decision Date2005-02-01
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES is the device name listed in this FDA 510(k) record. The listed applicant is Westcon Contact Lens Co., Inc.. It received FDA 510(k) clearance on 2005-02-01 under 510(k) number K043540. 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 HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES?

HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES is a medical device that received FDA 510(k) clearance on 2005-02-01. The listed applicant is Westcon Contact Lens Co., Inc.. The 510(k) number is K043540.

When did HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES receive FDA 510(k) clearance?

HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES received FDA 510(k) clearance on 2005-02-01, under 510(k) number K043540.

Who is the listed applicant for HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES?

The FDA 510(k) record lists Westcon Contact Lens Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES?

The FDA product code for HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES is LPL.

Related Clinical Trials

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.

Other records listing Westcon Contact Lens Co., Inc. 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.

View all 9 devices →

Related Devices (Code: LPL)

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.

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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