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FDA 510(k)

NEW EDITIONS CHILDRENS SUNGLASSES

K-Number: K922370 · 1993-03-19

Decision Date1993-03-19
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NEW EDITIONS CHILDRENS SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Fishel Toys , Ltd.. It received FDA 510(k) clearance on 1993-03-19 under 510(k) number K922370. 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 NEW EDITIONS CHILDRENS SUNGLASSES?

NEW EDITIONS CHILDRENS SUNGLASSES is a medical device that received FDA 510(k) clearance on 1993-03-19. The listed applicant is Fishel Toys , Ltd.. The 510(k) number is K922370.

When did NEW EDITIONS CHILDRENS SUNGLASSES receive FDA 510(k) clearance?

NEW EDITIONS CHILDRENS SUNGLASSES received FDA 510(k) clearance on 1993-03-19, under 510(k) number K922370.

Who is the listed applicant for NEW EDITIONS CHILDRENS SUNGLASSES?

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

What is the FDA product code for NEW EDITIONS CHILDRENS SUNGLASSES?

The FDA product code for NEW EDITIONS CHILDRENS 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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