DISCO SUNGLASSES/HEADBAND SUNGLASSES
K-Number: K832564 · 1983-09-12
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Device Summary
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
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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