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FDA 510(k)

VISTAKON (SENOFILCON A) SOFT CONTACT LENS

K-Number: K042275 · 2004-10-28

ApplicantVistakon
Decision Date2004-10-28
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISTAKON (SENOFILCON A) SOFT CONTACT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Vistakon. It received FDA 510(k) clearance on 2004-10-28 under 510(k) number K042275. 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 VISTAKON (SENOFILCON A) SOFT CONTACT LENS?

VISTAKON (SENOFILCON A) SOFT CONTACT LENS is a medical device that received FDA 510(k) clearance on 2004-10-28. The listed applicant is Vistakon. The 510(k) number is K042275.

When did VISTAKON (SENOFILCON A) SOFT CONTACT LENS receive FDA 510(k) clearance?

VISTAKON (SENOFILCON A) SOFT CONTACT LENS received FDA 510(k) clearance on 2004-10-28, under 510(k) number K042275.

Who is the listed applicant for VISTAKON (SENOFILCON A) SOFT CONTACT LENS?

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

What is the FDA product code for VISTAKON (SENOFILCON A) SOFT CONTACT LENS?

The FDA product code for VISTAKON (SENOFILCON A) 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 Vistakon 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

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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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