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FDA 510(k)

MARS SUNGLASSES

K-Number: K932484 · 1994-07-25

Decision Date1994-07-25
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MARS SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Mars Promotional Services, Inc.. It received FDA 510(k) clearance on 1994-07-25 under 510(k) number K932484. 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 MARS SUNGLASSES?

MARS SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-07-25. The listed applicant is Mars Promotional Services, Inc.. The 510(k) number is K932484.

When did MARS SUNGLASSES receive FDA 510(k) clearance?

MARS SUNGLASSES received FDA 510(k) clearance on 1994-07-25, under 510(k) number K932484.

Who is the listed applicant for MARS SUNGLASSES?

The FDA 510(k) record lists Mars Promotional Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARS SUNGLASSES?

The FDA product code for MARS 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.

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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