SUNGLASSES, NONPRESCRIPTION
K-Number: K951131 · 1995-05-10
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Device Summary
Frequently Asked Questions
What is the SUNGLASSES, NONPRESCRIPTION?
SUNGLASSES, NONPRESCRIPTION is a medical device that received FDA 510(k) clearance on 1995-05-10. The listed applicant is Gold, Inc.. The 510(k) number is K951131.
When did SUNGLASSES, NONPRESCRIPTION receive FDA 510(k) clearance?
SUNGLASSES, NONPRESCRIPTION received FDA 510(k) clearance on 1995-05-10, under 510(k) number K951131.
Who is the listed applicant for SUNGLASSES, NONPRESCRIPTION?
The FDA 510(k) record lists Gold, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUNGLASSES, NONPRESCRIPTION?
The FDA product code for SUNGLASSES, NONPRESCRIPTION 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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