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FDA 510(k)

CHILDREN'S SUNGLASSES

K-Number: K901468 · 1990-05-03

Decision Date1990-05-03
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CHILDREN'S SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is M. & S. Shillman, Inc.. It received FDA 510(k) clearance on 1990-05-03 under 510(k) number K901468. 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 CHILDREN'S SUNGLASSES?

CHILDREN'S SUNGLASSES is a medical device that received FDA 510(k) clearance on 1990-05-03. The listed applicant is M. & S. Shillman, Inc.. The 510(k) number is K901468.

When did CHILDREN'S SUNGLASSES receive FDA 510(k) clearance?

CHILDREN'S SUNGLASSES received FDA 510(k) clearance on 1990-05-03, under 510(k) number K901468.

Who is the listed applicant for CHILDREN'S SUNGLASSES?

The FDA 510(k) record lists M. & S. Shillman, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHILDREN'S SUNGLASSES?

The FDA product code for CHILDREN'S 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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