W-55 (METHAFILON A) CONTACT LENS
K-Number: K954524 · 1996-03-28
Advertisement
Device Summary
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.
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.
Advertisement