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FDA 510(k)

MARCHON/MARCOLIN SUNGLASSES

K-Number: K933734 · 1993-09-20

Decision Date1993-09-20
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MARCHON/MARCOLIN SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Marchon Eyewear, Inc.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K933734. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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

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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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