FDA 510(k)

HORIZON/WESTHIN 55-G

K-Number: K962121 · 1996-08-26

Decision Date1996-08-26

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

HORIZON/WESTHIN 55-G 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 1996-08-26 under 510(k) number K962121. 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/WESTHIN 55-G?

HORIZON/WESTHIN 55-G is a medical device that received FDA 510(k) clearance on 1996-08-26. The listed applicant is Westcon Contact Lens Co., Inc.. The 510(k) number is K962121.

When did HORIZON/WESTHIN 55-G receive FDA 510(k) clearance?

HORIZON/WESTHIN 55-G received FDA 510(k) clearance on 1996-08-26, under 510(k) number K962121.

Who is the listed applicant for HORIZON/WESTHIN 55-G?

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/WESTHIN 55-G?

The FDA product code for HORIZON/WESTHIN 55-G is LPL.

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Other records listing Westcon Contact Lens Co., Inc. as applicant

K043540HORIZON 59 OASIS (HIOXIFILCON A) DAILY WEAR CONTACT LENSES K031774HORIZON (METHAFILCON A) DAILY WEAR SPHERE AND TORIC CONTACT LENSES K023530HORIZON 38 (CLEAR) AND HORIZON 38 WESTINT (TINTED)K992010W-55 (METHAFILCON A) CLEAR AND VISIBILITY TINTED LENS BLANK AND HORIZON 55 SOFT (CLEAR) AND HORIZON 55 WESTINT (TINTED)K963837HORIZON/WESTHIN 38 SOFBLU (POLYMACON) SOFT (SPHERICAL & TORIC) DAILY WEAR CONTACT LENS (TINTED, LATHE-CUT FROM LENS BLAN K954524W-55 (METHAFILON A) CONTACT LENS

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Related Devices (Code: LPL)

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.