HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES
K-Number: K043540 · 2005-02-01
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Device Summary
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.
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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