EYE CARE CURE CONTACT LENS CASE
K-Number: K112832 · 2011-12-05
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Device Summary
Frequently Asked Questions
What is the EYE CARE CURE CONTACT LENS CASE?
EYE CARE CURE CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 2011-12-05. The listed applicant is Eye Care and Cure. The 510(k) number is K112832.
When did EYE CARE CURE CONTACT LENS CASE receive FDA 510(k) clearance?
EYE CARE CURE CONTACT LENS CASE received FDA 510(k) clearance on 2011-12-05, under 510(k) number K112832.
Who is the listed applicant for EYE CARE CURE CONTACT LENS CASE?
The FDA 510(k) record lists Eye Care and Cure as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EYE CARE CURE CONTACT LENS CASE?
The FDA product code for EYE CARE CURE 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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