HORIZON 55 BI-CON
K-Number: K945365 · 1994-12-28
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Device Summary
Frequently Asked Questions
What is the HORIZON 55 BI-CON?
HORIZON 55 BI-CON is a medical device that received FDA 510(k) clearance on 1994-12-28. The listed applicant is Westcon Contact Lens Co., Inc.. The 510(k) number is K945365.
When did HORIZON 55 BI-CON receive FDA 510(k) clearance?
HORIZON 55 BI-CON received FDA 510(k) clearance on 1994-12-28, under 510(k) number K945365.
Who is the listed applicant for HORIZON 55 BI-CON?
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 55 BI-CON?
The FDA product code for HORIZON 55 BI-CON 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.
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