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FDA 510(k)

DISCO SUNGLASSES/HEADBAND SUNGLASSES

K-Number: K832564 · 1983-09-12

Decision Date1983-09-12
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DISCO SUNGLASSES/HEADBAND SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is E-Tay Industrial Co. , Ltd.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832564. 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/HEADBAND SUNGLASSES?

DISCO SUNGLASSES/HEADBAND SUNGLASSES is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is E-Tay Industrial Co. , Ltd.. The 510(k) number is K832564.

When did DISCO SUNGLASSES/HEADBAND SUNGLASSES receive FDA 510(k) clearance?

DISCO SUNGLASSES/HEADBAND SUNGLASSES received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832564.

Who is the listed applicant for DISCO SUNGLASSES/HEADBAND SUNGLASSES?

The FDA 510(k) record lists E-Tay Industrial Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISCO SUNGLASSES/HEADBAND SUNGLASSES?

The FDA product code for DISCO SUNGLASSES/HEADBAND 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

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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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