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FDA 510(k)

VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS

K-Number: K953804 · 1995-09-26

Decision Date1995-09-26
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Vistakon, Johnson & Johnson Vision Products, Inc.. It received FDA 510(k) clearance on 1995-09-26 under 510(k) number K953804. 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 MULTIFOCAL (ETAFILCON A) CONTACT LENS?

VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS is a medical device that received FDA 510(k) clearance on 1995-09-26. The listed applicant is Vistakon, Johnson & Johnson Vision Products, Inc.. The 510(k) number is K953804.

When did VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS receive FDA 510(k) clearance?

VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS received FDA 510(k) clearance on 1995-09-26, under 510(k) number K953804.

Who is the listed applicant for VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS?

The FDA 510(k) record lists Vistakon, Johnson & Johnson Vision Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISTAKON MULTIFOCAL (ETAFILCON A) CONTACT LENS?

The FDA product code for VISTAKON MULTIFOCAL (ETAFILCON A) 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, Johnson & Johnson Vision Products, 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.

View all 8 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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