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FDA 510(k)

SPECTACLE FRAMES/SUNGLASSES

K-Number: K954419 · 1996-05-16

ApplicantAmi Fashion
Decision Date1996-05-16
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE FRAMES/SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Ami Fashion. It received FDA 510(k) clearance on 1996-05-16 under 510(k) number K954419. 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 SPECTACLE FRAMES/SUNGLASSES?

SPECTACLE FRAMES/SUNGLASSES is a medical device that received FDA 510(k) clearance on 1996-05-16. The listed applicant is Ami Fashion. The 510(k) number is K954419.

When did SPECTACLE FRAMES/SUNGLASSES receive FDA 510(k) clearance?

SPECTACLE FRAMES/SUNGLASSES received FDA 510(k) clearance on 1996-05-16, under 510(k) number K954419.

Who is the listed applicant for SPECTACLE FRAMES/SUNGLASSES?

The FDA 510(k) record lists Ami Fashion as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTACLE FRAMES/SUNGLASSES?

The FDA product code for SPECTACLE FRAMES/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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