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FDA 510(k)

DISCO SUNGLASSES (NON-PRESCRIPTION)

K-Number: K900387 · 1990-02-28

Decision Date1990-02-28
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DISCO SUNGLASSES (NON-PRESCRIPTION) is the device name listed in this FDA 510(k) record. The listed applicant is Le-I Electronic Co. , Ltd.. It received FDA 510(k) clearance on 1990-02-28 under 510(k) number K900387. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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