MARCHON/MARCOLIN SUNGLASSES
K-Number: K933734 · 1993-09-20
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Device Summary
Frequently Asked Questions
What is the MARCHON/MARCOLIN SUNGLASSES?
MARCHON/MARCOLIN SUNGLASSES is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Marchon Eyewear, Inc.. The 510(k) number is K933734.
When did MARCHON/MARCOLIN SUNGLASSES receive FDA 510(k) clearance?
MARCHON/MARCOLIN SUNGLASSES received FDA 510(k) clearance on 1993-09-20, under 510(k) number K933734.
Who is the listed applicant for MARCHON/MARCOLIN SUNGLASSES?
The FDA 510(k) record lists Marchon Eyewear, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MARCHON/MARCOLIN SUNGLASSES?
The FDA product code for MARCHON/MARCOLIN SUNGLASSES is HQY.
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 Marchon Eyewear, 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: HQY)
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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