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FDA 510(k)

DAILIES (NELFILCON A) ONE-DAY SOFT CONTACT LENS

K-Number: K963487 · 1996-11-27

Decision Date1996-11-27
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DAILIES (NELFILCON A) ONE-DAY SOFT CONTACT LENS 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 1996-11-27 under 510(k) number K963487. 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 DAILIES (NELFILCON A) ONE-DAY SOFT CONTACT LENS?

DAILIES (NELFILCON A) ONE-DAY SOFT CONTACT LENS is a medical device that received FDA 510(k) clearance on 1996-11-27. The listed applicant is Ciba Vision Corporation. The 510(k) number is K963487.

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

DAILIES (NELFILCON A) ONE-DAY SOFT CONTACT LENS received FDA 510(k) clearance on 1996-11-27, under 510(k) number K963487.

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

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 DAILIES (NELFILCON A) ONE-DAY SOFT CONTACT LENS?

The FDA product code for DAILIES (NELFILCON A) ONE-DAY SOFT CONTACT LENS 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.

View all 43 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

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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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