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FDA 510(k)

BUFFARD CREATION (SUNGLASSES)

K-Number: K955933 · 1996-03-04

Decision Date1996-03-04
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BUFFARD CREATION (SUNGLASSES) is the device name listed in this FDA 510(k) record. The listed applicant is Buffard Creation Eurl. It received FDA 510(k) clearance on 1996-03-04 under 510(k) number K955933. 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 BUFFARD CREATION (SUNGLASSES)?

BUFFARD CREATION (SUNGLASSES) is a medical device that received FDA 510(k) clearance on 1996-03-04. The listed applicant is Buffard Creation Eurl. The 510(k) number is K955933.

When did BUFFARD CREATION (SUNGLASSES) receive FDA 510(k) clearance?

BUFFARD CREATION (SUNGLASSES) received FDA 510(k) clearance on 1996-03-04, under 510(k) number K955933.

Who is the listed applicant for BUFFARD CREATION (SUNGLASSES)?

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

What is the FDA product code for BUFFARD CREATION (SUNGLASSES)?

The FDA product code for BUFFARD CREATION (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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