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FDA 510(k)

HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED)

K-Number: K023530 · 2002-11-26

Decision Date2002-11-26
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED) is the device name listed in this FDA 510(k) record. The listed applicant is Westcon Contact Lens Co., Inc.. It received FDA 510(k) clearance on 2002-11-26 under 510(k) number K023530. 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 HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED)?

HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED) is a medical device that received FDA 510(k) clearance on 2002-11-26. The listed applicant is Westcon Contact Lens Co., Inc.. The 510(k) number is K023530.

When did HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED) receive FDA 510(k) clearance?

HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED) received FDA 510(k) clearance on 2002-11-26, under 510(k) number K023530.

Who is the listed applicant for HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED)?

The FDA 510(k) record lists Westcon Contact Lens Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED)?

The FDA product code for HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED) 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 Westcon Contact Lens Co., 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 9 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

View on FDA Database →

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

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