ORVIS KEY WEST SUNGLASSES
K-Number: K950609 · 1995-03-02
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Device Summary
Frequently Asked Questions
What is the ORVIS KEY WEST SUNGLASSES?
ORVIS KEY WEST SUNGLASSES is a medical device that received FDA 510(k) clearance on 1995-03-02. The listed applicant is The Orvis Co., Inc.. The 510(k) number is K950609.
When did ORVIS KEY WEST SUNGLASSES receive FDA 510(k) clearance?
ORVIS KEY WEST SUNGLASSES received FDA 510(k) clearance on 1995-03-02, under 510(k) number K950609.
Who is the listed applicant for ORVIS KEY WEST SUNGLASSES?
The FDA 510(k) record lists The Orvis Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ORVIS KEY WEST SUNGLASSES?
The FDA product code for ORVIS KEY WEST 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 The Orvis Co., Inc. 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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