NON-PRESCRIPTION SUNGLASSES
K-Number: K900936 · 1990-06-22
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Device Summary
Frequently Asked Questions
What is the NON-PRESCRIPTION SUNGLASSES?
NON-PRESCRIPTION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1990-06-22. The listed applicant is Barkley House, Inc.. The 510(k) number is K900936.
When did NON-PRESCRIPTION SUNGLASSES receive FDA 510(k) clearance?
NON-PRESCRIPTION SUNGLASSES received FDA 510(k) clearance on 1990-06-22, under 510(k) number K900936.
Who is the listed applicant for NON-PRESCRIPTION SUNGLASSES?
The FDA 510(k) record lists Barkley House, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-PRESCRIPTION SUNGLASSES?
The FDA product code for NON-PRESCRIPTION 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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