NON-PRESCRIPTION EYEGLASS FRAMES & SUNGLASSES VARIOUS STYLES
K-Number: K934120 · 1993-10-18
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Device Summary
Frequently Asked Questions
What is the NON-PRESCRIPTION EYEGLASS FRAMES & SUNGLASSES VARIOUS STYLES?
NON-PRESCRIPTION EYEGLASS FRAMES & SUNGLASSES VARIOUS STYLES is a medical device that received FDA 510(k) clearance on 1993-10-18. The listed applicant is Lux DE Paris, Inc.. The 510(k) number is K934120.
When did NON-PRESCRIPTION EYEGLASS FRAMES & SUNGLASSES VARIOUS STYLES receive FDA 510(k) clearance?
NON-PRESCRIPTION EYEGLASS FRAMES & SUNGLASSES VARIOUS STYLES received FDA 510(k) clearance on 1993-10-18, under 510(k) number K934120.
Who is the listed applicant for NON-PRESCRIPTION EYEGLASS FRAMES & SUNGLASSES VARIOUS STYLES?
The FDA 510(k) record lists Lux DE Paris, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-PRESCRIPTION EYEGLASS FRAMES & SUNGLASSES VARIOUS STYLES?
The FDA product code for NON-PRESCRIPTION EYEGLASS FRAMES & SUNGLASSES VARIOUS STYLES 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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