DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES
K-Number: K934309 · 1993-11-02
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Device Summary
Frequently Asked Questions
What is the DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES?
DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is U.S. Toy Co., Inc.. The 510(k) number is K934309.
When did DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES receive FDA 510(k) clearance?
DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES received FDA 510(k) clearance on 1993-11-02, under 510(k) number K934309.
Who is the listed applicant for DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES?
The FDA 510(k) record lists U.S. Toy Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISCO SUNGLASSES NONPRESCRIPTION SUNGLASSES?
The FDA product code for DISCO SUNGLASSES NONPRESCRIPTION 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.
Other records listing U.S. Toy Co., 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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