ALL KINDS OF SUNGLASSES
K-Number: K853921 · 1985-10-15
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Device Summary
Frequently Asked Questions
What is the ALL KINDS OF SUNGLASSES?
ALL KINDS OF SUNGLASSES is a medical device that received FDA 510(k) clearance on 1985-10-15. The listed applicant is Winsburn Company , Ltd.. The 510(k) number is K853921.
When did ALL KINDS OF SUNGLASSES receive FDA 510(k) clearance?
ALL KINDS OF SUNGLASSES received FDA 510(k) clearance on 1985-10-15, under 510(k) number K853921.
Who is the listed applicant for ALL KINDS OF SUNGLASSES?
The FDA 510(k) record lists Winsburn Company , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALL KINDS OF SUNGLASSES?
The FDA product code for ALL KINDS OF 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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