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FDA 510(k)

W-55 (METHAFILON A) CONTACT LENS

K-Number: K954524 · 1996-03-28

Decision Date1996-03-28
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

W-55 (METHAFILON A) CONTACT LENS 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 1996-03-28 under 510(k) number K954524. 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 W-55 (METHAFILON A) CONTACT LENS?

W-55 (METHAFILON A) CONTACT LENS is a medical device that received FDA 510(k) clearance on 1996-03-28. The listed applicant is Westcon Contact Lens Co., Inc.. The 510(k) number is K954524.

When did W-55 (METHAFILON A) CONTACT LENS receive FDA 510(k) clearance?

W-55 (METHAFILON A) CONTACT LENS received FDA 510(k) clearance on 1996-03-28, under 510(k) number K954524.

Who is the listed applicant for W-55 (METHAFILON A) CONTACT LENS?

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 W-55 (METHAFILON A) CONTACT LENS?

The FDA product code for W-55 (METHAFILON 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 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

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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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