VISARD SUNGLASSES
K-Number: K961117 · 1996-04-24
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Device Summary
Frequently Asked Questions
What is the VISARD SUNGLASSES?
VISARD SUNGLASSES is a medical device that received FDA 510(k) clearance on 1996-04-24. The listed applicant is Visard Srl. The 510(k) number is K961117.
When did VISARD SUNGLASSES receive FDA 510(k) clearance?
VISARD SUNGLASSES received FDA 510(k) clearance on 1996-04-24, under 510(k) number K961117.
Who is the listed applicant for VISARD SUNGLASSES?
The FDA 510(k) record lists Visard Srl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VISARD SUNGLASSES?
The FDA product code for VISARD 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.
Other records listing Visard Srl as applicant
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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