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FDA 510(k)

RUSSELL & HANCOCK 524 AND 422 SUNGLASSES

K-Number: K933323 · 1993-12-21

ApplicantRussell & Hancock, Ltd.
Decision Date1993-12-21
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RUSSELL & HANCOCK 524 AND 422 SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Russell & Hancock, Ltd.. It received FDA 510(k) clearance on 1993-12-21 under 510(k) number K933323. 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 RUSSELL & HANCOCK 524 AND 422 SUNGLASSES?

RUSSELL & HANCOCK 524 AND 422 SUNGLASSES is a medical device that received FDA 510(k) clearance on 1993-12-21. The listed applicant is Russell & Hancock, Ltd.. The 510(k) number is K933323.

When did RUSSELL & HANCOCK 524 AND 422 SUNGLASSES receive FDA 510(k) clearance?

RUSSELL & HANCOCK 524 AND 422 SUNGLASSES received FDA 510(k) clearance on 1993-12-21, under 510(k) number K933323.

Who is the listed applicant for RUSSELL & HANCOCK 524 AND 422 SUNGLASSES?

The FDA 510(k) record lists Russell & Hancock, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RUSSELL & HANCOCK 524 AND 422 SUNGLASSES?

The FDA product code for RUSSELL & HANCOCK 524 AND 422 SUNGLASSES is HQY.

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Related Devices (Code: HQY)

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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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