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FDA 510(k)

THE OPTIC BOX CONTACT LENS CASE

K-Number: K895167 · 1990-01-22

Decision Date1990-01-22
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE OPTIC BOX CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is The Optic Box Co., Ltd.. It received FDA 510(k) clearance on 1990-01-22 under 510(k) number K895167. 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 THE OPTIC BOX CONTACT LENS CASE?

THE OPTIC BOX CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is The Optic Box Co., Ltd.. The 510(k) number is K895167.

When did THE OPTIC BOX CONTACT LENS CASE receive FDA 510(k) clearance?

THE OPTIC BOX CONTACT LENS CASE received FDA 510(k) clearance on 1990-01-22, under 510(k) number K895167.

Who is the listed applicant for THE OPTIC BOX CONTACT LENS CASE?

The FDA 510(k) record lists The Optic Box Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE OPTIC BOX CONTACT LENS CASE?

The FDA product code for THE OPTIC BOX 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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