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FDA 510(k)

FLAT SLIP-IN SUNGLASSES

K-Number: K903719 · 1990-10-11

Decision Date1990-10-11
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FLAT SLIP-IN SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Yorktowne Optical Co., Inc.. It received FDA 510(k) clearance on 1990-10-11 under 510(k) number K903719. 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 FLAT SLIP-IN SUNGLASSES?

FLAT SLIP-IN SUNGLASSES is a medical device that received FDA 510(k) clearance on 1990-10-11. The listed applicant is Yorktowne Optical Co., Inc.. The 510(k) number is K903719.

When did FLAT SLIP-IN SUNGLASSES receive FDA 510(k) clearance?

FLAT SLIP-IN SUNGLASSES received FDA 510(k) clearance on 1990-10-11, under 510(k) number K903719.

Who is the listed applicant for FLAT SLIP-IN SUNGLASSES?

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

What is the FDA product code for FLAT SLIP-IN SUNGLASSES?

The FDA product code for FLAT SLIP-IN 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 Yorktowne Optical 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

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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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