ALIBI OPTICAL FRAMES AND SUNGLASSES
K-Number: K925187 · 1993-10-01
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Device Summary
Frequently Asked Questions
What is the ALIBI OPTICAL FRAMES AND SUNGLASSES?
ALIBI OPTICAL FRAMES AND SUNGLASSES is a medical device that received FDA 510(k) clearance on 1993-10-01. The listed applicant is Alibi Designs, Inc.. The 510(k) number is K925187.
When did ALIBI OPTICAL FRAMES AND SUNGLASSES receive FDA 510(k) clearance?
ALIBI OPTICAL FRAMES AND SUNGLASSES received FDA 510(k) clearance on 1993-10-01, under 510(k) number K925187.
Who is the listed applicant for ALIBI OPTICAL FRAMES AND SUNGLASSES?
The FDA 510(k) record lists Alibi Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALIBI OPTICAL FRAMES AND SUNGLASSES?
The FDA product code for ALIBI OPTICAL FRAMES AND 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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