THE OPTIC BOX CONTACT LENS CASE
K-Number: K895167 · 1990-01-22
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement