OPTI-RAY SUNGLASSES
K-Number: K902414 · 1990-07-17
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Device Summary
Frequently Asked Questions
What is the OPTI-RAY SUNGLASSES?
OPTI-RAY SUNGLASSES is a medical device that received FDA 510(k) clearance on 1990-07-17. The listed applicant is Opti-Ray, Inc.. The 510(k) number is K902414.
When did OPTI-RAY SUNGLASSES receive FDA 510(k) clearance?
OPTI-RAY SUNGLASSES received FDA 510(k) clearance on 1990-07-17, under 510(k) number K902414.
Who is the listed applicant for OPTI-RAY SUNGLASSES?
The FDA 510(k) record lists Opti-Ray, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPTI-RAY SUNGLASSES?
The FDA product code for OPTI-RAY 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 Opti-Ray, 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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