NON-PRESCRIPTION SUNGLASSES
K-Number: K896768 · 1989-12-26
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Device Summary
Frequently Asked Questions
What is the NON-PRESCRIPTION SUNGLASSES?
NON-PRESCRIPTION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1989-12-26. The listed applicant is Shairon Intl. Trade Co.. The 510(k) number is K896768.
When did NON-PRESCRIPTION SUNGLASSES receive FDA 510(k) clearance?
NON-PRESCRIPTION SUNGLASSES received FDA 510(k) clearance on 1989-12-26, under 510(k) number K896768.
Who is the listed applicant for NON-PRESCRIPTION SUNGLASSES?
The FDA 510(k) record lists Shairon Intl. Trade Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-PRESCRIPTION SUNGLASSES?
The FDA product code for NON-PRESCRIPTION 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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