Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES

K-Number: K003586 · 2001-02-08

Decision Date2001-02-08
Product CodeMVN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES is the device name listed in this FDA 510(k) record. The listed applicant is Ciba-Geigy Corp.. It received FDA 510(k) clearance on 2001-02-08 under 510(k) number K003586. The device is classified under product code MVN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES?

FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES is a medical device that received FDA 510(k) clearance on 2001-02-08. The listed applicant is Ciba-Geigy Corp.. The 510(k) number is K003586.

When did FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES receive FDA 510(k) clearance?

FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES received FDA 510(k) clearance on 2001-02-08, under 510(k) number K003586.

Who is the listed applicant for FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES?

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

What is the FDA product code for FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES?

The FDA product code for FOCUS DAILIES (NELFILCON A) ONE-DAY CONTACT LENSES is MVN.

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-Geigy Corp. 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: MVN)

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.

↑