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FDA 510(k)

ALIBI OPTICAL FRAMES AND SUNGLASSES

K-Number: K925187 · 1993-10-01

Decision Date1993-10-01
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ALIBI OPTICAL FRAMES AND SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Alibi Designs, Inc.. It received FDA 510(k) clearance on 1993-10-01 under 510(k) number K925187. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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