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FDA 510(k)

AC LENS BRANDED CONTACT LENS CASE

K-Number: K120969 · 2012-07-11

Decision Date2012-07-11
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AC LENS BRANDED CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Arlington Contact Lens Services,Inc.. It received FDA 510(k) clearance on 2012-07-11 under 510(k) number K120969. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AC LENS BRANDED CONTACT LENS CASE?

AC LENS BRANDED CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 2012-07-11. The listed applicant is Arlington Contact Lens Services,Inc.. The 510(k) number is K120969.

When did AC LENS BRANDED CONTACT LENS CASE receive FDA 510(k) clearance?

AC LENS BRANDED CONTACT LENS CASE received FDA 510(k) clearance on 2012-07-11, under 510(k) number K120969.

Who is the listed applicant for AC LENS BRANDED CONTACT LENS CASE?

The FDA 510(k) record lists Arlington Contact Lens Services,Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AC LENS BRANDED CONTACT LENS CASE?

The FDA product code for AC LENS BRANDED 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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