CONTACT LENS CASE FOR RIGID GAS PERMA
K-Number: K840691 · 1984-05-18
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Device Summary
Frequently Asked Questions
What is the CONTACT LENS CASE FOR RIGID GAS PERMA?
CONTACT LENS CASE FOR RIGID GAS PERMA is a medical device that received FDA 510(k) clearance on 1984-05-18. The listed applicant is Optimum Manufacturers, Inc.. The 510(k) number is K840691.
When did CONTACT LENS CASE FOR RIGID GAS PERMA receive FDA 510(k) clearance?
CONTACT LENS CASE FOR RIGID GAS PERMA received FDA 510(k) clearance on 1984-05-18, under 510(k) number K840691.
Who is the listed applicant for CONTACT LENS CASE FOR RIGID GAS PERMA?
The FDA 510(k) record lists Optimum Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONTACT LENS CASE FOR RIGID GAS PERMA?
The FDA product code for CONTACT LENS CASE FOR RIGID GAS PERMA 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.
Other records listing Optimum Manufacturers, Inc. as applicant
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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