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FDA 510(k)

TONKA BOYS SUNGLASSES

K-Number: K944328 · 1994-10-03

Decision Date1994-10-03
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TONKA BOYS SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Hasbro Industries, Inc.. It received FDA 510(k) clearance on 1994-10-03 under 510(k) number K944328. 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 TONKA BOYS SUNGLASSES?

TONKA BOYS SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-10-03. The listed applicant is Hasbro Industries, Inc.. The 510(k) number is K944328.

When did TONKA BOYS SUNGLASSES receive FDA 510(k) clearance?

TONKA BOYS SUNGLASSES received FDA 510(k) clearance on 1994-10-03, under 510(k) number K944328.

Who is the listed applicant for TONKA BOYS SUNGLASSES?

The FDA 510(k) record lists Hasbro Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TONKA BOYS SUNGLASSES?

The FDA product code for TONKA BOYS 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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