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FDA 510(k)

TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES

K-Number: K961523 · 1996-05-13

ApplicantDorda Toys
Decision Date1996-05-13
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Dorda Toys. It received FDA 510(k) clearance on 1996-05-13 under 510(k) number K961523. 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 TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES?

TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES is a medical device that received FDA 510(k) clearance on 1996-05-13. The listed applicant is Dorda Toys. The 510(k) number is K961523.

When did TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES receive FDA 510(k) clearance?

TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES received FDA 510(k) clearance on 1996-05-13, under 510(k) number K961523.

Who is the listed applicant for TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES?

The FDA 510(k) record lists Dorda Toys as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES?

The FDA product code for TINY TOON SUNGLASSES & CABBAGE PATCH KIDS SUNGLASSES is HQY.

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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.

K974852NON-PRESCRIPTION SUNGLASSESChia Hui Spectacles Mfg. Corp.K974860NON-PRESCRIPTION SUNGLASSESWenzhou Ming Ming Optical Co. , Ltd.K974861NON-PRESCRIPTION SUNGLASSESWenzhou Hindar Optical Co., Ltd.K974511SUNGLASSESSun World Intl., Inc.K974441SUNGLASSESHip Shing Fat Co., Ltd.K973528SUNGLASSESJeou Jeou Long Industrial Co., Ltd.

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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