I-PROMOTIONS CONTACT LENS CASE
K-Number: K042578 · 2005-01-25
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Device Summary
Frequently Asked Questions
What is the I-PROMOTIONS CONTACT LENS CASE?
I-PROMOTIONS CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 2005-01-25. The listed applicant is I-Promotions, Inc.. The 510(k) number is K042578.
When did I-PROMOTIONS CONTACT LENS CASE receive FDA 510(k) clearance?
I-PROMOTIONS CONTACT LENS CASE received FDA 510(k) clearance on 2005-01-25, under 510(k) number K042578.
Who is the listed applicant for I-PROMOTIONS CONTACT LENS CASE?
The FDA 510(k) record lists I-Promotions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for I-PROMOTIONS CONTACT LENS CASE?
The FDA product code for I-PROMOTIONS 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.
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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