NEW EDITIONS CHILDRENS SUNGLASSES
K-Number: K922370 · 1993-03-19
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Device Summary
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
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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