CIBA VISION(R) CONTACT LENS CASE
K-Number: K943183 · 1994-08-04
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Device Summary
Frequently Asked Questions
What is the CIBA VISION(R) CONTACT LENS CASE?
CIBA VISION(R) CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1994-08-04. The listed applicant is Ciba Vision Corporation. The 510(k) number is K943183.
When did CIBA VISION(R) CONTACT LENS CASE receive FDA 510(k) clearance?
CIBA VISION(R) CONTACT LENS CASE received FDA 510(k) clearance on 1994-08-04, under 510(k) number K943183.
Who is the listed applicant for CIBA VISION(R) CONTACT LENS CASE?
The FDA 510(k) record lists Ciba Vision Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CIBA VISION(R) CONTACT LENS CASE?
The FDA product code for CIBA VISION(R) CONTACT LENS CASE is LRX.
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 Ciba Vision Corporation 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: LRX)
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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