SUNGLASS, NON-PRESCRIPTION
K-Number: K900764 · 1990-06-20
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Device Summary
Frequently Asked Questions
What is the SUNGLASS, NON-PRESCRIPTION?
SUNGLASS, NON-PRESCRIPTION is a medical device that received FDA 510(k) clearance on 1990-06-20. The listed applicant is Seiko Optical Products of America, Inc.. The 510(k) number is K900764.
When did SUNGLASS, NON-PRESCRIPTION receive FDA 510(k) clearance?
SUNGLASS, NON-PRESCRIPTION received FDA 510(k) clearance on 1990-06-20, under 510(k) number K900764.
Who is the listed applicant for SUNGLASS, NON-PRESCRIPTION?
The FDA 510(k) record lists Seiko Optical Products of America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUNGLASS, NON-PRESCRIPTION?
The FDA product code for SUNGLASS, NON-PRESCRIPTION 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 Seiko Optical Products of America, 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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