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FDA 510(k)

CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSES

K-Number: K073459 · 2008-02-28

Decision Date2008-02-28
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSES 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 2008-02-28 under 510(k) number K073459. 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 CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSES?

CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSES is a medical device that received FDA 510(k) clearance on 2008-02-28. The listed applicant is Ciba Vision Corporation. The 510(k) number is K073459.

When did CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSES receive FDA 510(k) clearance?

CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSES received FDA 510(k) clearance on 2008-02-28, under 510(k) number K073459.

Who is the listed applicant for CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSES?

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 CIBA VISION (LOTRAFILCON B) SOFT CONTACT LENSES?

The FDA product code for CIBA VISION (LOTRAFILCON B) SOFT 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 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.

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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

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

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