BUFFARD CREATION (SUNGLASSES)
K-Number: K955933 · 1996-03-04
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Device Summary
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
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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