DISCO SUNGLASSES (NON-PRESCRIPTION)
K-Number: K900387 · 1990-02-28
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Device Summary
Frequently Asked Questions
What is the DISCO SUNGLASSES (NON-PRESCRIPTION)?
DISCO SUNGLASSES (NON-PRESCRIPTION) is a medical device that received FDA 510(k) clearance on 1990-02-28. The listed applicant is Le-I Electronic Co. , Ltd.. The 510(k) number is K900387.
When did DISCO SUNGLASSES (NON-PRESCRIPTION) receive FDA 510(k) clearance?
DISCO SUNGLASSES (NON-PRESCRIPTION) received FDA 510(k) clearance on 1990-02-28, under 510(k) number K900387.
Who is the listed applicant for DISCO SUNGLASSES (NON-PRESCRIPTION)?
The FDA 510(k) record lists Le-I Electronic Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISCO SUNGLASSES (NON-PRESCRIPTION)?
The FDA product code for DISCO SUNGLASSES (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.
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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